CN103485213A - Formaldehyde-free discharging agent and preparation method thereof - Google Patents
Formaldehyde-free discharging agent and preparation method thereof Download PDFInfo
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- CN103485213A CN103485213A CN201310397672.6A CN201310397672A CN103485213A CN 103485213 A CN103485213 A CN 103485213A CN 201310397672 A CN201310397672 A CN 201310397672A CN 103485213 A CN103485213 A CN 103485213A
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Abstract
The invention relates to the leather processing field, and in particular relates to a formaldehyde-free discharging agent and a preparation method thereof. The formaldehyde-free discharging agent is composed of the following components in parts by weight: 10-50 parts of first compound, 2-10 parts of penetrant and 10-30 parts of solid organic acid; the preparation method of the formaldehyde-free discharging agent comprises the following steps: adding 10-30 parts of solid organic acid to 10-50 parts of first compound and mixing evenly; heating to 20-30 DEG C, adding 2-10 parts of penetrate and for stirring for 10-20 minutes. The formaldehyde-free discharging agent provided by the invention does not cause any harmful substance formaldehyde to be generated or left while performing discharging on fur. Simultaneously, the preparation method of the formaldehyde-free discharging agent provided by the invention is simple in synthesis process and environment-friendly.
Description
Technical field
The present invention relates to the leather processing field, in particular to without aldehyde pulling color agent and preparation method thereof.
Background technology
On fur grass in the market, the pulling color agent of frost making use be take sodium formaldehyde sulfoxylate as main.
Although its, effect was better dawn, can produce the harmful substances such as formaldehyde in its use procedure.Diazolidinyl Urea in the pulling color operating process, endanger the healthy of operator simultaneously, and the residual a large amount of formaldehyde of meeting on the fur after dawn, and the harm user's is healthy.
Summary of the invention
The object of the present invention is to provide without aldehyde pulling color agent and preparation method thereof, to solve the above problems.
Provide in an embodiment of the present invention without the agent of aldehyde pulling color, in parts by weight, by following component, made:
First compound 10-50 part; Bleeding agent 2-10 part; Solid organic acid 10-30 part; The molecular formula of described the first compound is
Without the preparation method of aldehyde pulling color agent, comprise following concrete steps:
The solid organic acid that adds 10-30 part in first compound of 10-50 part, mix; The molecular formula of described the first compound is
Be heated to 20-30 ℃, add the bleeding agent of 2-10 part to stir 10-20 minute.
Reductant the first compound used in the present invention is to be replaced as organic group R at the part inorganic group by strand in existing sodium dithionite
1, R
2, R
3those skilled in the art can directly obtain this method of replacing by the relevant knowledge of having controlled, can stable existence after the first compound after displacement is water-soluble, and not carrying aldehyde radical, the first compound does not have harmful substance formaldehyde generation or residual when as reductant, fur being carried out to pulling color.Because the pH value of solution can not be too high when pulling color, not so can injure fur simultaneously, cause the hair on fur to come off, so, need to add solid organic acid.Be in order to increase the infiltration of reductant on fur and add bleeding agent, increase the dawn degree.
Preparation method's synthesis technique without the agent of aldehyde pulling color provided by the invention is simple simultaneously, environmental protection.
The accompanying drawing explanation
The preparation method's flow chart without the agent of aldehyde pulling color that Fig. 1 provides for the embodiment of the present invention 1;
The preparation method's flow chart without the agent of aldehyde pulling color that Fig. 2 provides for the embodiment of the present invention 2;
The preparation method's flow chart without the agent of aldehyde pulling color that Fig. 3 provides for the embodiment of the present invention 3;
The preparation method's flow chart without the agent of aldehyde pulling color that Fig. 4 provides for the embodiment of the present invention 4;
The preparation method's flow chart without the agent of aldehyde pulling color that Fig. 5 provides for the embodiment of the present invention 5;
The preparation method's flow chart without the agent of aldehyde pulling color that Fig. 6 provides for the embodiment of the present invention 6.
The specific embodiment
Below by specific embodiment, also by reference to the accompanying drawings the present invention is described in further detail.
Embodiment 1:
Without the agent of aldehyde pulling color, in parts by weight, by following component, made:
First compound 10-50 part; Bleeding agent 2-10 part; Solid organic acid 10-30 part; The molecular formula of described the first compound is
The preparation method without the agent of aldehyde pulling color as shown in Figure 1 comprises following concrete steps:
101. the solid organic acid that adds 10-30 part in first compound of 10-50 part, mix; The molecular formula of described the first compound is
102. be heated to 20-30 ℃, add the bleeding agent of 2-10 part to stir 10-20 minute.
Reductant the first compound used in the present invention is to be replaced as organic group R at the part inorganic group by strand in existing sodium dithionite
1, R
2, R
3those skilled in the art can directly obtain this method of replacing by the relevant knowledge of having controlled, can stable existence after the first compound after displacement is water-soluble, and not carrying aldehyde radical, the first compound does not have harmful substance formaldehyde generation or residual when as reductant, fur being carried out to pulling color.Because the pH value of solution can not be too high when pulling color, not so can injure fur simultaneously, cause the hair on fur to come off, so, need to add solid organic acid.Be in order to increase the infiltration of reductant on fur and add bleeding agent, increase the dawn degree.
Preparation method's synthesis technique without the agent of aldehyde pulling color provided by the invention is simple simultaneously, environmental protection.
Embodiment 2: the preparation method without the agent of aldehyde pulling color as shown in Figure 2 comprises following concrete steps:
201. first compounds of 50 parts and 5 parts of citric acids are added in container successively, mix the R in the molecular formula of wherein said the first compound
1base and R
2base is methyl, R
3base is the carboxylic acid sodium group;
202. temperature is remained on to 25 ℃, add the JFC of 5 parts, stir while adding, stir 10 minutes, obtain target product.
Embodiment 3: the preparation method without the agent of aldehyde pulling color as shown in Figure 3 comprises following concrete steps:
301. the ascorbic acid of first compounds of 30 parts and 6 parts is added in container successively, mixes the R in the molecular formula of wherein said the first compound
1base is hydroxyl, R
2base is methyl, R
3base is the carboxylic acid sodium group;
302. temperature is remained on to 25 ℃, add the glycerine of 10 parts, add while stirring, stir 15 minutes, obtain target product.
Embodiment 4: the preparation method without the agent of aldehyde pulling color as shown in Figure 4 comprises following concrete steps:
401. first compounds of 10 parts and 20 parts of tartaric acid are added in container successively, mix the R in the molecular formula of wherein said the first compound
1base is hydroxyl, R
2base is phenyl, R
3base is the carboxylic acid sodium group;
402. temperature is remained on to 25 ℃, in whipping process, add while stirring 8 parts of urea in the container of mix reagent, stir 15 minutes, obtain target product.
Embodiment 5: the preparation method without the agent of aldehyde pulling color as shown in Figure 5 comprises following concrete steps:
501. first compounds of 20 parts and 20 parts of glutamic acid are added in container successively, mix the R in the molecular formula of wherein said the first compound
1base is ethyl, R
2base is phenyl, R
3base is the carboxylic acid sodium group;
502. temperature is remained on to 25 ℃, in whipping process, add while stirring the ethylene glycol of 6 parts in the container of mix reagent, stir 15 minutes, obtain target product.
Embodiment 6: the preparation method without the agent of aldehyde pulling color as shown in Figure 6 comprises following concrete steps:
601. first compounds of 40 parts and 15 parts of arabo-ascorbic acids are added in container successively, mix the R in the molecular formula of wherein said the first compound
1base is ethyl, R
2base is phenyl, R
3base is the carboxylic acid sodium group;
602. temperature is remained on to 25 ℃, in whipping process, add while stirring the propylene glycol of 6 parts in the container of mix reagent, stir 15 minutes, obtain target product.
The foregoing is only the preferred embodiments of the present invention, be not limited to the present invention, for a person skilled in the art, the present invention can have various modifications and variations.Within the spirit and principles in the present invention all, any modification of doing, be equal to replacement, improvement etc., within all should being included in protection scope of the present invention.
Claims (9)
1. without the agent of aldehyde pulling color, it is characterized in that, in parts by weight, made by following component:
First compound 10-50 part; Bleeding agent 2-10 part; Solid organic acid 10-30 part; The molecular formula of described the first compound is
2. according to claim 1ly without the agent of aldehyde pulling color, it is characterized in that, in parts by weight, made by following component:
First compound 20-40 part; Bleeding agent 5-10 part; Solid organic acid 15-25 part.
3. according to claim 1 and 2ly without the agent of aldehyde pulling color, it is characterized in that,
R in the molecular formula of described the first compound
1base, R
2base, R
3base is respectively any in hydrogen, methyl, ethyl, phenyl, carboxyl, oh group.
4. according to claim 1 and 2ly without the agent of aldehyde pulling color, it is characterized in that,
Described bleeding agent be in JFC, glycerine, ethylene glycol, urea, propylene glycol any one or multiple.
5. according to claim 1 and 2ly without the agent of aldehyde pulling color, it is characterized in that,
Described solid organic acid is ascorbic acid, arabo-ascorbic acid, citric acid, any one in tartaric acid, glutamic acid or multiple.
6. without the preparation method of aldehyde pulling color agent, it is characterized in that, comprise following concrete steps:
The solid organic acid that adds 10-30 part in first compound of 10-50 part, mix; The molecular formula of described the first compound is
Be heated to 20-30 ℃, add the bleeding agent of 2-10 part to stir 10-20 minute.
7. the preparation method without the agent of aldehyde pulling color according to claim 6, is characterized in that,
R in the molecular formula of described the first compound
1base, R
2base, R
3base is respectively any in hydrogen, methyl, ethyl, phenyl, carboxyl, oh group.
8. the preparation method without the agent of aldehyde pulling color according to claim 6, is characterized in that,
Described bleeding agent be in JFC, glycerine, ethylene glycol, urea, propylene glycol any one or multiple.
9. the preparation method without the agent of aldehyde pulling color according to claim 6, is characterized in that,
Described solid organic acid is ascorbic acid, arabo-ascorbic acid, citric acid, any one in tartaric acid, glutamic acid or multiple.
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104264517A (en) * | 2014-10-13 | 2015-01-07 | 北京泛博化学股份有限公司 | Bicolored dyeing method for rabbit fur |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1237156A (en) * | 1997-10-02 | 1999-12-01 | L·布鲁克曼两合公司 | Sulphinic acid derivatives, method for producing them, and their use |
US20020138920A1 (en) * | 2001-04-02 | 2002-10-03 | Anthony Pepitone | Process for printing textile material |
CN102304861A (en) * | 2011-07-18 | 2012-01-04 | 南通思瑞纺织品后整理有限公司 | Cotton-containing garment color stripping process comprising sand blasting |
CN102704292A (en) * | 2012-05-25 | 2012-10-03 | 浙江理工大学 | Environment-friendly paste discharge agent for textile printing and preparation method thereof |
-
2013
- 2013-09-04 CN CN201310397672.6A patent/CN103485213B/en active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1237156A (en) * | 1997-10-02 | 1999-12-01 | L·布鲁克曼两合公司 | Sulphinic acid derivatives, method for producing them, and their use |
US20020138920A1 (en) * | 2001-04-02 | 2002-10-03 | Anthony Pepitone | Process for printing textile material |
CN102304861A (en) * | 2011-07-18 | 2012-01-04 | 南通思瑞纺织品后整理有限公司 | Cotton-containing garment color stripping process comprising sand blasting |
CN102704292A (en) * | 2012-05-25 | 2012-10-03 | 浙江理工大学 | Environment-friendly paste discharge agent for textile printing and preparation method thereof |
Non-Patent Citations (1)
Title |
---|
张桂珍等: "一步式多套拔染印花人造毛皮工艺研究", 《针织工业》 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104264517A (en) * | 2014-10-13 | 2015-01-07 | 北京泛博化学股份有限公司 | Bicolored dyeing method for rabbit fur |
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