CN106283748B - A kind of textile printing and dyeing environmentally protective food grade acidity body and preparation method thereof - Google Patents

A kind of textile printing and dyeing environmentally protective food grade acidity body and preparation method thereof Download PDF

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Publication number
CN106283748B
CN106283748B CN201610562860.3A CN201610562860A CN106283748B CN 106283748 B CN106283748 B CN 106283748B CN 201610562860 A CN201610562860 A CN 201610562860A CN 106283748 B CN106283748 B CN 106283748B
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Prior art keywords
parts
dyeing
textile
citric acid
added
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CN106283748A (en
Inventor
付吉广
付宾
刘珊
付慧
王超
商艳红
杨珂
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Jining Jinxiang Technology Development Co Ltd
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Jining Jinxiang Technology Development Co Ltd
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Priority to CN201610562860.3A priority Critical patent/CN106283748B/en
Publication of CN106283748A publication Critical patent/CN106283748A/en
Priority to PCT/CN2017/092765 priority patent/WO2018014775A1/en
Priority to AU2017299652A priority patent/AU2017299652B2/en
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/653Nitrogen-free carboxylic acids or their salts
    • D06P1/6533Aliphatic, araliphatic or cycloaliphatic
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/653Nitrogen-free carboxylic acids or their salts
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/673Inorganic compounds
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/673Inorganic compounds
    • D06P1/67333Salts or hydroxides
    • D06P1/6735Salts or hydroxides of alkaline or alkaline-earth metals with anions different from those provided for in D06P1/67341

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Coloring (AREA)

Abstract

The present invention relates to a kind of textile printing and dyeing environmentally protective food grade acidity bodies and preparation method thereof;Belong to technical field of textile printing.The acid body of the present invention, raw material and parts by weight are:56 68 parts of 26 36 parts of deionized water, 4.6 6.8 parts of potassium hydrogen peroxymonosulfate, 10 16 parts of light-coloured vinegar and citric acid.Nontoxic, safe and environment-friendly, edible, and compared with citric acid, have price advantage;Loose colour can preferably be complexed, keep the color of textile more gorgeous, bright;Without additional addition soaping agent when use;The metal ions such as calcium, magnesium, arsenic, lead, Gong in water quality can be complexed, make product safety, nontoxic;So that the surface of the textile after printing and dyeing does not have one layer of white;With stronger dirt-removing power, can prevent by variegated pollution;The good color fastness of treated textile, it is colour-fast;Can effectively prevent treated, textile causes secondary pollution to other products in use.

Description

A kind of textile printing and dyeing environmentally protective food grade acidity body and preparation method thereof
Technical field
The present invention relates to a kind of textile printing and dyeing environmentally protective food grade acidity bodies and preparation method thereof;Belong to textile printing and dyeing Technical field.
Background technology
Currently, the kind of the dyeing acid used during textile printing and dyeing has:Sulfuric acid, synthesis acid(Dyeing acid), technical grade Glacial acetic acid;No matter these product category dangerous material bring greatly inconvenient and insecurity in terms of transport and business administration.And And existed to human body insecurity using above-mentioned dyeing acid in textile and dyeing industry;Such as, in operation, above-mentioned dyeing Acid, which splashes, causes burn, scald to leave permanent scar on worker's skin, splash the event in worker's eyes and happen occasionally and cause Life-long disabilities.People is more allowed to worry, the medical textile products prepared at present using above-mentioned dyeing acid(Medical absorbent cotton, medical yarn Cloth, medical cotton ball, medical cotton stick etc.)Heavy metal, such as arsenic, lead, Gong are usually contained, food grade security level is not achieved.
Invention content
The purpose of the present invention is to provide a kind of environmentally protective food grades of efficient, environmentally friendly, nontoxic, safe textile printing and dyeing Acid body;To substitute existing dyeing acid, and it can realize, even preferably effect suitable with existing dyeing acid.
The present invention also provides the textile printing and dyeing preparation methods of environmentally protective food grade acidity body.
Technical solution
A kind of environmentally protective food grade acidity body of textile printing and dyeing, raw material and parts by weight are:26-36 parts of deionized water, 56-68 parts of 4.6-6.8 parts of potassium hydrogen peroxymonosulfate, 10-16 parts of light-coloured vinegar and citric acid.
The potassium hydrogen peroxymonosulfate, also known as Potassium Monopersulfate, molecular formula are KHSO5
The light-coloured vinegar is the tart flavour auxiliary material cooked, color and luster is bright, tart flavour alcohol just;The acetic acid and water of the 3-5% containing mass concentration.
The citric acid, white crystalline powder.
The environmentally protective food grade acidity body of above-mentioned textile printing and dyeing, preferably constitute for:26 parts of deionized water, permonosulphuric acid 60 parts of 4.6 parts of hydrogen potassium, 16 parts of light-coloured vinegar and citric acid.
Light-coloured vinegar and citric acid are food grade materials so that product of the invention is environmentally friendly, nontoxic, edible.Light-coloured vinegar and lemon Lemon acid coordinates, and on the one hand citric acid can be enable to be completely dissolved, prevent dissolved lemon acid crystal(Lemon acid crystal can cause Filament damage), on the other hand can surprisingly play effect of preferably soaping.
The above-mentioned textile printing and dyeing preparation method of environmentally protective food grade acidity body, includes the following steps:
In a kettle, 100-120 DEG C is warming up to after potassium hydrogen peroxymonosulfate being dissolved in deionized water, heat preservation 46 DEG C are cooled to after 28min;Then light-coloured vinegar is added and stirs 6min, adds citric acid, capping kettle, heat preservation 48min.
Above-mentioned preparation method, in order to make potassium hydrogen peroxymonosulfate quickly be dissolved in deionized water, preferably by deionized water Potassium hydrogen peroxymonosulfate, and the insulated and stirred 26min after potassium hydrogen peroxymonosulfate is added are added after being heated to 46 DEG C.
Above-mentioned preparation method, the purpose of " potassium hydrogen peroxymonosulfate is warming up to 100-120 DEG C after being dissolved in deionized water " It is:The acid body of preparation is set to have excellent sterilization, disinfection, insect prevention, anti-mildew effect.
Above-mentioned preparation method, each temperature parameter are by being obtained after many experiments;The institute only under this temperature parameter The properties of the acid body of preparation could meet the requirement of " suitable with existing dyeing acid, even preferably effect ".
The environmentally protective food grade acidity body of above-mentioned textile printing and dyeing, as dyeing acid, in the dyeing process of textile; Use temperature range:30-80℃;Dosage:0.5-1kg acidity body/100kg textiles.
Advantageous effect
The acid body of the present invention:
1, nontoxic, safe and environment-friendly, edible, and compared with citric acid, have price advantage;
2, effect of soaping is good:Loose colour can preferably be complexed, keep the color of textile more gorgeous, bright;Volume is not necessarily to when use Outer addition soaping agent;
3, the metal ions such as calcium, magnesium, arsenic, lead, Gong in water quality are complexed, make product safety, nontoxic;So that the spinning after printing and dyeing The surface of fabric does not have one layer of white;
4, there is stronger dirt-removing power, remaining color dirt impurity dye can be prevented;
5, the good color fastness of treated textile, it is colour-fast;The textile that can effectively prevent that treated is using process In secondary pollution is caused to other products.
Specific implementation mode
Embodiment 1
Deionized water 26kg, potassium hydrogen peroxymonosulfate 4.6kg, light-coloured vinegar 10kg and citric acid 56kg.
Deionized water is added in reaction kettle, is opened and is stirred and be warming up to 46 DEG C;Potassium hydrogen peroxymonosulfate is added, stir, It is continuously heating to 100 DEG C after heat preservation 26min;It is cooled to 46 DEG C after stirring, heat preservation 28min;Be added light-coloured vinegar, stir 6min after slowly Citric acid is added;Add citric acid rear enclosed reaction kettle, stirring, heat preservation 48min;It can be obtained acid body.The acidity obtained Body, under normal temperature condition, exposed to air will not crystallize placing 96 days.
Embodiment 2
Deionized water 26kg, potassium hydrogen peroxymonosulfate 6.8kg, light-coloured vinegar 16kg and citric acid 68kg.
Deionized water is added in reaction kettle, is opened and is stirred and be warming up to 46 DEG C;Potassium hydrogen peroxymonosulfate is added, stir, It is continuously heating to 100 DEG C after heat preservation 26min;It is cooled to 46 DEG C after stirring, heat preservation 28min;Be added light-coloured vinegar, stir 6min after slowly Citric acid is added;Add citric acid rear enclosed reaction kettle, stirring, heat preservation 48min;It can be obtained acid body.The acidity obtained Body, under normal temperature condition, exposed to air will not crystallize placing 96 days.
Embodiment 3
Deionized water 26kg, potassium hydrogen peroxymonosulfate 4.6kg, light-coloured vinegar 16kg and citric acid 60kg.
Deionized water is added in reaction kettle, is opened and is stirred and be warming up to 46 DEG C;Potassium hydrogen peroxymonosulfate is added, stir, It is continuously heating to 100 DEG C after heat preservation 26min;It is cooled to 46 DEG C after stirring, heat preservation 28min;Be added light-coloured vinegar, stir 6min after slowly Citric acid is added;Add citric acid rear enclosed reaction kettle, stirring, heat preservation 48min;It can be obtained acid body.The acidity obtained Body, under normal temperature condition, exposed to air will not crystallize placing 96 days.
Embodiment 4
Deionized water 36kg, potassium hydrogen peroxymonosulfate 4.6kg, light-coloured vinegar 10kg and citric acid 56kg.
Deionized water is added in reaction kettle, is opened and is stirred and be warming up to 46 DEG C;Potassium hydrogen peroxymonosulfate is added, stir, It is continuously heating to 100 DEG C after heat preservation 26min;It is cooled to 46 DEG C after stirring, heat preservation 28min;Be added light-coloured vinegar, stir 6min after slowly Citric acid is added;Add citric acid rear enclosed reaction kettle, stirring, heat preservation 48min;It can be obtained acid body.The acidity obtained Body, under normal temperature condition, exposed to air will not crystallize placing 96 days.
Embodiment 5
Deionized water 36kg, potassium hydrogen peroxymonosulfate 6.8kg, light-coloured vinegar 16kg and citric acid 68kg.
Deionized water is added in reaction kettle, is opened and is stirred and be warming up to 46 DEG C;Potassium hydrogen peroxymonosulfate is added, stir, It is continuously heating to 100 DEG C after heat preservation 26min;It is cooled to 46 DEG C after stirring, heat preservation 28min;Be added light-coloured vinegar, stir 6min after slowly Citric acid is added;Add citric acid rear enclosed reaction kettle, stirring, heat preservation 48min;It can be obtained acid body.The acidity obtained Body, under normal temperature condition, exposed to air will not crystallize placing 96 days.
Embodiment 6
Deionized water 26kg, potassium hydrogen peroxymonosulfate 4.6kg, light-coloured vinegar 10kg and citric acid 56kg.
Deionized water is added in reaction kettle, is opened and is stirred and be warming up to 46 DEG C;Potassium hydrogen peroxymonosulfate is added, stir, It is continuously heating to 120 DEG C after heat preservation 26min;It is cooled to 46 DEG C after stirring, heat preservation 28min;Be added light-coloured vinegar, stir 6min after slowly Citric acid is added;Add citric acid rear enclosed reaction kettle, stirring, heat preservation 48min;It can be obtained acid body.The acidity obtained Body, under normal temperature condition, exposed to air will not crystallize placing 96 days.
Comparative example 1
Deionized water 26kg, light-coloured vinegar 10kg and citric acid 56kg.
Deionized water is added in reaction kettle, is opened and is stirred and be warming up to 46 DEG C;Be added light-coloured vinegar, stir 6min after slowly Citric acid is added;Add citric acid rear enclosed reaction kettle, stirring, heat preservation 48min;It can be obtained acid body.The acidity obtained Body, under normal temperature condition, exposed to air will not crystallize placing 96 days.
Comparative example 2
Deionized water 26kg, potassium hydrogen peroxymonosulfate 4.6kg and citric acid 56kg.
Deionized water is added in reaction kettle, is opened and is stirred and be warming up to 46 DEG C;Potassium hydrogen peroxymonosulfate is added, stir, It is continuously heating to 100 DEG C after heat preservation 26min;It is cooled to 46 DEG C after stirring, heat preservation 28min;Citric acid is added;After adding citric acid Capping kettle, stirring, heat preservation 48min;It can be obtained acid body.There is crystallization in the acid body obtained;In normal temperature condition Under, exposed to air, after placing 1 day, crystalline content improves 9.6%.
Comparative example 3
Deionized water 26kg, citric acid 56kg.
Deionized water is added in reaction kettle, is opened and is stirred and be warming up to 46 DEG C;Citric acid is added;After adding citric acid Capping kettle, stirring, heat preservation 48min;It can be obtained acid body.There is crystallization in the acid body obtained;In normal temperature condition Under, exposed to air, after placing 2 hours, crystalline content improves 16.8%.
Comparative example 4
Using the sulfuric acid solution that mass concentration is 38% as acid body.
Embodiment 7
(1)Acid body prepared by embodiment 1-6, comparative example 1-4 is respectively adopted, using following dyeing conditions to stained clot-h into Row dyeing.Dyeing condition:The red B-4BD of dye activity, dosage 6%(Quality relative to stained clot-h);Acid body, dosage 1%(Phase For the quality of stained clot-h);Water consumption is 10 liters of water/1Kg stained clot-hs;Bath raio is:1:10;Other auxiliary materials be anhydrous sodium sulphate, soda ash, Deoxygenase, dosage mutually should be:50g/ rises water, 25g/ rises water, 0.1g/ rises water;130 DEG C of temperature;Time 15min.Stained clot-h is taken out, In 130 DEG C of drying.
(2)Treated that stained clot-h is primary with cold rinse respectively by dyed, the depth of observation drift foot-washing water, as a result such as Table 1.
(3)By the stained clot-h by rinsing processing, in 130 DEG C of drying;Then color fastness to washing experimental method GB/ is pressed respectively T 3921-2008 and colour fasteness to sunlight GB/T 8427-2008 test its color fastness;The results are shown in Table 1.
Table 1

Claims (2)

1. a kind of environmentally protective food grade acidity body of textile printing and dyeing, which is characterized in that its raw material and parts by weight are:Deionized water 56-68 parts of 26-36 parts, 4.6-6.8 parts of potassium hydrogen peroxymonosulfate, 10-16 parts of light-coloured vinegar and citric acid;
Preparation method includes the following steps:
Deionized water is added in reaction kettle, stir and is warming up to 46 DEG C;Potassium hydrogen peroxymonosulfate, stirring, heat preservation 26min is added After be continuously heating to 100-120 DEG C;It is cooled to 46 DEG C after stirring, heat preservation 28min;Light-coloured vinegar is added, stirs 6min, lemon is added Acid, capping kettle, stirring, heat preservation 48min.
2. the environmentally protective food grade acidity body of textile printing and dyeing according to claim 1, which is characterized in that deionized water 26 Part, 4.6 parts of potassium hydrogen peroxymonosulfate, 16 parts of light-coloured vinegar and 60 parts of citric acid.
CN201610562860.3A 2016-07-18 2016-07-18 A kind of textile printing and dyeing environmentally protective food grade acidity body and preparation method thereof Active CN106283748B (en)

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CN201610562860.3A CN106283748B (en) 2016-07-18 2016-07-18 A kind of textile printing and dyeing environmentally protective food grade acidity body and preparation method thereof
PCT/CN2017/092765 WO2018014775A1 (en) 2016-07-18 2017-07-13 Environmentally-friendly food grade acidic body for textile printing and dyeing and preparation method therefor
AU2017299652A AU2017299652B2 (en) 2016-07-18 2017-07-13 Environmentally-friendly food grade acidic body for textile printing and dyeing and preparation method therefor

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Publication number Priority date Publication date Assignee Title
CN106283748B (en) * 2016-07-18 2018-08-21 济宁锦祥科技发展有限公司 A kind of textile printing and dyeing environmentally protective food grade acidity body and preparation method thereof
CN107837210A (en) * 2017-11-15 2018-03-27 济宁锦祥科技发展有限公司 A kind of pollution-free food level disinfection hand cleanser

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1033469A (en) * 1987-12-08 1989-06-21 新疆阜康助剂厂 A kind of acid colouring agent
CN101302711A (en) * 2008-06-20 2008-11-12 杭州下沙恒升化工有限公司 Solid tasteless odorless acid agent for textile dyeing and finishing process

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1054627A (en) * 1990-03-05 1991-09-18 孙德和 The preparation method of uniform dyeing compound organic acid-staining acid
JPH04316687A (en) * 1991-04-08 1992-11-09 Kanebo Ltd Coloring of cellulosic fiber structure containing protein fiber
CN1263964A (en) * 1999-02-13 2000-08-23 黄成勋 Dyeing acid
CN101906726B (en) * 2010-08-19 2012-10-24 中国纺织科学研究院 Method for dyeing modified polyester
CN102108641B (en) * 2011-01-12 2012-09-05 郑州鸿盛数码科技股份有限公司 Digital printing active dye jet ink
CN104404709A (en) * 2014-09-03 2015-03-11 江苏阳光集团有限公司 Production process for anti-ultraviolet radiation fabric
CN105623873A (en) * 2015-12-29 2016-06-01 辛集市远翔环保能源科技有限公司 Cleaning agent for removing pesticide residues on fruits
CN106283748B (en) * 2016-07-18 2018-08-21 济宁锦祥科技发展有限公司 A kind of textile printing and dyeing environmentally protective food grade acidity body and preparation method thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1033469A (en) * 1987-12-08 1989-06-21 新疆阜康助剂厂 A kind of acid colouring agent
CN101302711A (en) * 2008-06-20 2008-11-12 杭州下沙恒升化工有限公司 Solid tasteless odorless acid agent for textile dyeing and finishing process

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