CN105347717A - Composite water reducing agent - Google Patents
Composite water reducing agent Download PDFInfo
- Publication number
- CN105347717A CN105347717A CN201410411710.3A CN201410411710A CN105347717A CN 105347717 A CN105347717 A CN 105347717A CN 201410411710 A CN201410411710 A CN 201410411710A CN 105347717 A CN105347717 A CN 105347717A
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- CN
- China
- Prior art keywords
- raw material
- reducing agent
- water reducing
- water
- water reducer
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- 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.)
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Abstract
The present invention belongs to the technical field of water reducing agents, and particularly relates to a composite reducing agent, which comprises an organic water reducing agent raw material and an inorganic water reducing agent raw material according to a ratio of 1:1-2. According to the present invention, the prepared water reducing agent has advantages of good decondensation effect, wide decondensation range, energy saving, effect increase, easy use and the like, and is the ideal building ceramic mud slurry dilution assisted-grinding material.
Description
Technical field
The invention belongs to water reducer technical field, be specifically related to a kind of composite water-reducing agent.
Background technology
Reduce the water content the spray drying granulation efficiency improving mud of building blank mud, thus reach reduction production cost, the object of energy efficient is the problem that current building industry needs to solve always.For this reason, current building ceramics factory commonly uses the suitable mud water reducer meeting property of raw material detritus acid sodium, lignosulfite, sodium polyacrylate etc.But at present the water-reducing effect of water reducer that generally uses of China's building trade is not ideal enough, the water content major part of mud between 40-45%, and also exists water reducer and adds narrow range, the shortcoming that thixotropy is large.
Summary of the invention
The object of the invention is to solve above-mentioned technical problem and a kind of composite water-reducing agent and preparation method thereof is provided.
The present invention is achieved in that a kind of composite water-reducing agent, comprising:
Organic water reducer raw material;
Inorganic water reducer raw material;
Above-mentioned organic water reducer raw material, the ratio of components of inorganic water reducer raw material are 1: 1-2.
Described organic water reducer raw material comprises anion surfactant sodium laurylsulfonate and or cats product Australia cetyl pyridinium.
Described inorganic water reducer raw material comprises water glass or sodium carbonate.
The concrete preparation process of above-mentioned water reducer comprises the following steps:
By above-mentioned raw materials respectively according to organic water reducer: inorganic water reducer be 1: 1-2 proportioning be configured, mixed by ball milling at normal temperatures, obtained composite water-reducing agent.
Water reducer prepared by the present invention, have separate solidifying effective, separate the advantages such as solidifying wide ranges, energy efficiency and user make, be desirable architectural pottery mud dilution grinding aid material.
Embodiment
Below, in conjunction with example, substantive distinguishing features of the present invention and advantage are further described, but the present invention is not limited to listed embodiment.
Embodiment one
(1) 50g sodium laurylsulfonate and 50g water glass is selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment two
(1) 50g sodium laurylsulfonate and 60g water glass is selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment three
(1) 50g sodium laurylsulfonate and 70g water glass is selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment four
(1) 50g sodium laurylsulfonate and 75 water glass are selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment five
(1) 50g sodium laurylsulfonate and 80g water glass is selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment six
(1) 50g sodium laurylsulfonate and 85g water glass is selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment seven
(1) 50g sodium laurylsulfonate and 90 water glass are selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment eight
(1) 50g sodium laurylsulfonate and 100g water glass is selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment nine
(1) 50g Australia cetyl pyridinium and 50g sodium carbonate is selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment ten
(1) 50g Australia cetyl pyridinium and 60g sodium carbonate is selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment 11
(1) 50g Australia cetyl pyridinium and 70g sodium carbonate is selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment 12
(1) 50g brocide and 75g sodium carbonate is selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment 13
(1) 50g Australia cetyl pyridinium and 80g sodium carbonate is selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment 14
(1) 50g brocide and 90g sodium carbonate is selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Embodiment 15
(1) 50g Australia cetyl pyridinium and 100g sodium carbonate is selected to be raw material;
(2) join directly good raw material mixed above-mentioned by ball milling at normal temperatures.
Claims (3)
1. a composite water-reducing agent, is characterized in that, comprising:
Organic water reducer raw material;
Inorganic water reducer raw material;
Above-mentioned organic water reducer raw material, the ratio of components of inorganic water reducer raw material are 1: 1-2.
2. composite water-reducing agent as claimed in claim 1, is characterized in that, described organic water reducer raw material comprises anion surfactant sodium laurylsulfonate and or cats product Australia cetyl pyridinium.
3. composite water-reducing agent as claimed in claim 1, is characterized in that, described inorganic water reducer raw material comprises water glass and or sodium carbonate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410411710.3A CN105347717A (en) | 2014-08-18 | 2014-08-18 | Composite water reducing agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410411710.3A CN105347717A (en) | 2014-08-18 | 2014-08-18 | Composite water reducing agent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN105347717A true CN105347717A (en) | 2016-02-24 |
Family
ID=55323812
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201410411710.3A Pending CN105347717A (en) | 2014-08-18 | 2014-08-18 | Composite water reducing agent |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN105347717A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110372324A (en) * | 2019-08-27 | 2019-10-25 | 安徽恒杰新材料科技股份有限公司 | A kind of ceramics bentonite and preparation method thereof |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1821177A (en) * | 2006-03-08 | 2006-08-23 | 桂林工学院 | Method for preparing composite ceramic water reducing agent |
-
2014
- 2014-08-18 CN CN201410411710.3A patent/CN105347717A/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1821177A (en) * | 2006-03-08 | 2006-08-23 | 桂林工学院 | Method for preparing composite ceramic water reducing agent |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110372324A (en) * | 2019-08-27 | 2019-10-25 | 安徽恒杰新材料科技股份有限公司 | A kind of ceramics bentonite and preparation method thereof |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| WD01 | Invention patent application deemed withdrawn after publication | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20160224 |