CN103044674A - Preparation method of leveling agent - Google Patents
Preparation method of leveling agent Download PDFInfo
- Publication number
- CN103044674A CN103044674A CN2012105417159A CN201210541715A CN103044674A CN 103044674 A CN103044674 A CN 103044674A CN 2012105417159 A CN2012105417159 A CN 2012105417159A CN 201210541715 A CN201210541715 A CN 201210541715A CN 103044674 A CN103044674 A CN 103044674A
- Authority
- CN
- China
- Prior art keywords
- add
- preparation
- reaction
- pressure
- levelling agent
- 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.)
- Pending
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The present invention discloses a preparation method of a leveling agent, comprising the steps of: (1) feeding; (2) adding a catalyst; (3) adding EO for reaction; (4) post-processing; and (5) pressing, cooling and cutting into slices. Compared with the conventional preparation processes, the preparation method is higher in yield and less in process procedures.
Description
Technical field
The present invention is specifically related to a kind of preparation method of levelling agent.
Background technology
Levelling agent be fabric in dyeing course, for impelling even dyeing, do not produce the fault such as vitta, color spot and the material that adds, and the operation that general levelling agent preparation method needs is more, and output is not ideal enough.
Summary of the invention
Goal of the invention: the present invention provides the preparation method of the high levelling agent of a kind of production efficiency in order to solve the deficiencies in the prior art.
Technical scheme: for achieving the above object, the technical solution used in the present invention is as follows: a kind of preparation method of levelling agent, described preparation method comprises the following steps:
(1) feed intake: C16 ~ 18 alcohol are dropped into the stirring-type crucible, are to react 6-10h in 90-110 ℃ in temperature, are molten into liquid; (2) add catalyzer: the liquid negative pressure suction reactor with making in the step (1), add conventional basic catalyst, be warming up to 100-120 ℃, simultaneously negative pressure dehydration 40-60min;
(3) add EO reaction: at the 150-170 ℃ of lower EO reaction 4-6h that slowly adds, and pressure-controlling that will this moment drops to normal pressure with pressure after the reaction 30-60min, control during sampling is surveyed more than 0.4 MPa;
(4) aftertreatment: middle control data reach after the cloud point, cool to 120-130 ℃, add in the conventional acid and 10-30min, cool to 110-120 ℃, add discoloring agent again and process 10-30min;
(5) binder, cooling section: carry out binder after cooling to 90-110 ℃ and in reactor, cut into slices, last packing.As preferably, the mass ratio of described C16 ~ 18 pure and mild EO is 200-300:1000-1300.
As preferably, in the step (4), described cloud point is 91-94 ℃.
Beneficial effect: compared with prior art, operation is few, and output is higher.
Embodiment
Below the present invention will be described in detail.
Embodiment 1
A kind of preparation method of levelling agent, described preparation method comprises the following steps:
(1) feed intake: C16 ~ 18 alcohol are dropped into the stirring-type crucible, are to react 6h in 90 ℃ in temperature, are molten into liquid;
(2) add catalyzer: the liquid negative pressure suction reactor with making in the step (1), add conventional basic catalyst, be warming up to 100 ℃, simultaneously negative pressure dehydration 40min;
(3) add EO reaction: at 150 ℃ of lower EO reaction 4h that slowly add, and pressure-controlling that will this moment drops to normal pressure with pressure after the reaction 30min, control during sampling is surveyed more than 0.4 MPa;
(4) aftertreatment: middle control data reach after 91 ℃ of the cloud points, cool to 120 ℃, add in the conventional acid and 10min, cool to 110 ℃, add discoloring agent again and process 10min;
(5) binder, cooling section: carry out binder after cooling to 90 ℃ and in reactor, cut into slices, last packing.Among the present invention, the mass ratio of described C16 ~ 18 pure and mild EO is 200:1000.
Embodiment 2
A kind of preparation method of levelling agent, described preparation method comprises the following steps:
(1) feed intake: C16 ~ 18 alcohol are dropped into the stirring-type crucible, are to react 10h in 110 ℃ in temperature, are molten into liquid;
(2) add catalyzer: the liquid negative pressure suction reactor with making in the step (1), add conventional basic catalyst, be warming up to 120 ℃, simultaneously negative pressure dehydration 60min;
(3) add EO reaction: at 170 ℃ of lower EO reaction 6h that slowly add, and pressure-controlling that will this moment drops to normal pressure with pressure after the reaction 60min, control during sampling is surveyed more than 0.4 MPa;
(4) aftertreatment: middle control data reach after 94 ℃ of the cloud points, cool to 130 ℃, add in the conventional acid and 30min, cool to 120 ℃, add discoloring agent again and process 30min;
(5) binder, cooling section: carry out binder after cooling to 110 ℃ and in reactor, cut into slices, last packing.
Among the present invention, the mass ratio of described C16 ~ 18 pure and mild EO is 300:1300.
Embodiment 3
A kind of preparation method of levelling agent, described preparation method comprises the following steps:
(1) feed intake: C16 ~ 18 alcohol are dropped into the stirring-type crucible, are to react 8h in 100 ℃ in temperature, are molten into liquid;
(2) add catalyzer: the liquid negative pressure suction reactor with making in the step (1), add conventional basic catalyst, be warming up to 110 ℃, simultaneously negative pressure dehydration 55min;
(3) add EO reaction: at 160 ℃ of lower EO reaction 5h that slowly add, and pressure-controlling that will this moment drops to normal pressure with pressure after the reaction 50min, control during sampling is surveyed more than 0.4 MPa;
(4) aftertreatment: middle control data reach after 93 ℃ of the cloud points, cool to 125 ℃, add in the conventional acid and 20min, cool to 115 ℃, add discoloring agent again and process 20min;
(5) binder, cooling section: carry out binder after cooling to 100 ℃ and in reactor, cut into slices, last packing.
In the present invention, the mass ratio of described C16 ~ 18 pure and mild EO is 250:1200.
Claims (3)
1. the preparation method of a levelling agent, it is characterized in that: described preparation method comprises the following steps:
(1) feed intake: C16 ~ 18 alcohol are dropped into the stirring-type crucible, are to react 6-10h in 90-110 ℃ in temperature, are molten into liquid;
(2) add catalyzer: the liquid negative pressure suction reactor with making in the step (1), add conventional basic catalyst, be warming up to 100-120 ℃, simultaneously negative pressure dehydration 40-60min;
(3) add EO reaction: at the 150-170 ℃ of lower EO reaction 4-6h that slowly adds, and pressure-controlling that will this moment drops to normal pressure with pressure after the reaction 30-60min, control during sampling is surveyed more than 0.4 MPa;
(4) aftertreatment: middle control data reach after the cloud point, cool to 120-130 ℃, add in the conventional acid and 10-30min, cool to 110-120 ℃, add discoloring agent again and process 10-30min;
(5) binder, cooling section: carry out binder after cooling to 90-110 ℃ and in reactor, cut into slices, last packing.
2. the preparation method of levelling agent as claimed in claim 1, it is characterized in that: the mass ratio of described C16 ~ 18 pure and mild EO is 200-300:1000-1300.
3. the preparation method of levelling agent as claimed in claim 1, it is characterized in that: in the step (4), described cloud point is 91-94 ℃.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2012105417159A CN103044674A (en) | 2012-12-14 | 2012-12-14 | Preparation method of leveling agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2012105417159A CN103044674A (en) | 2012-12-14 | 2012-12-14 | Preparation method of leveling agent |
Publications (1)
Publication Number | Publication Date |
---|---|
CN103044674A true CN103044674A (en) | 2013-04-17 |
Family
ID=48057550
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2012105417159A Pending CN103044674A (en) | 2012-12-14 | 2012-12-14 | Preparation method of leveling agent |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN103044674A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1762948A (en) * | 2005-09-16 | 2006-04-26 | 陕西天宇制药有限公司 | Polycinnamic alcohol production formula and its preparation process |
CN101234953A (en) * | 2007-12-21 | 2008-08-06 | 王伟松 | Method for synthesizing hexade/octode mixing alcohol polyoxyethylene |
-
2012
- 2012-12-14 CN CN2012105417159A patent/CN103044674A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1762948A (en) * | 2005-09-16 | 2006-04-26 | 陕西天宇制药有限公司 | Polycinnamic alcohol production formula and its preparation process |
CN101234953A (en) * | 2007-12-21 | 2008-08-06 | 王伟松 | Method for synthesizing hexade/octode mixing alcohol polyoxyethylene |
Non-Patent Citations (1)
Title |
---|
百度百科: "平平加", 《HTTP://BAIKE.BAIDU.COM/HISTORY/31126685》 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101905157A (en) | Method for preparing mercury-free catalyst for preparing chloroethylene by acetylene hydrochlorination | |
CN103130182B (en) | A kind of method improving sodium borohydride hydrolysis hydrogen desorption capacity | |
CN102643160A (en) | Preparation method of 1,2,4-trifluorobenzene | |
CN103044674A (en) | Preparation method of leveling agent | |
CN102180900A (en) | Method for preparing bis(2,4,4-trimethylpentyl)phosphonic acid | |
CN103570498B (en) | A kind of glycerin chlorination prepares the method for dichlorohydrin | |
CN103436368A (en) | Method for synchronously preparing biodiesel and glycerol carbonate by using alkali-earth oxide as catalyst | |
CN102649057A (en) | Catalyst for preparing oxalate through coupling reaction of CO (carbon monoxide) | |
CN103480379A (en) | Method for preparing and synthetizing methanol catalyst from copper-based waste methanol catalyst recovered solution | |
CN203159225U (en) | Nitrogen making machine | |
CN204999870U (en) | Methyl alcohol synthetic LNG device of methanation of speeding to exit | |
CN103159175A (en) | High-conversion-rate germane preparation method | |
CN106632161A (en) | Method used for preparing gamma-valerolactone via high-selectivity catalysis | |
CN103232514A (en) | Preparation method of cortisone acetate | |
CN103772329B (en) | Method for simultaneous extraction and recovery of furfural and acetic acid from furfural stripping steam condensate | |
CN202199241U (en) | Recovery device of exhausted gas of synthesis ammonia and cuprammonia regenerative system comprising same | |
CN104892658A (en) | Preparation method of diphenyl difluorosilane | |
CN101250082A (en) | Preparation method of alpha-methylnaphthalene | |
CN103708996A (en) | Method for recycling methanol with rectification tower | |
CN103756715B (en) | A kind of preparation method of high-carbon hydrocarbon | |
CN103223343A (en) | Alkali metal modified copper-based catalyst for hydrogen production by dimethyl ether steam reforming and preparation method | |
CN102617338B (en) | Preparation method of p-trifluoromethyl salicylic acid | |
CN103113343B (en) | Prevent the treatment process of discolorment of vinylene carbonate | |
CN202322398U (en) | Novel device for synthesizing ammonia by using double-towel series connection technology | |
CN209652202U (en) | A kind of diacetone alcohol production system based on resin-column |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20130417 |