CN108342904A - A kind of creasing anti-bacterial processing method of real silk fabric - Google Patents
A kind of creasing anti-bacterial processing method of real silk fabric Download PDFInfo
- Publication number
- CN108342904A CN108342904A CN201810192484.2A CN201810192484A CN108342904A CN 108342904 A CN108342904 A CN 108342904A CN 201810192484 A CN201810192484 A CN 201810192484A CN 108342904 A CN108342904 A CN 108342904A
- Authority
- CN
- China
- Prior art keywords
- fabric
- solution
- wrinkle
- silk
- treatment method
- 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
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
- D06M15/6436—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing amino groups
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/07—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with halogens; with halogen acids or salts thereof; with oxides or oxyacids of halogens or salts thereof
- D06M11/11—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with halogens; with halogen acids or salts thereof; with oxides or oxyacids of halogens or salts thereof with halogen acids or salts thereof
- D06M11/155—Halides of elements of Groups 2 or 12 of the Periodic Table
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/73—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with carbon or compounds thereof
- D06M11/74—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with carbon or compounds thereof with carbon or graphite; with carbides; with graphitic acids or their salts
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/01—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
- D06M15/03—Polysaccharides or derivatives thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/02—Natural fibres, other than mineral fibres
- D06M2101/10—Animal fibres
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/20—Treatment influencing the crease behaviour, the wrinkle resistance, the crease recovery or the ironing ease
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
本发明提供了一种真丝织物的抗皱抗菌处理方法,壳聚糖本身具有明显的抗菌效果,生物相容性在改性后得到进一步提高,其次,改性后的有机硅整理剂可以进一步易产生褶皱的缺点,将石墨烯中的含氧集团与织物纤维结合之后织物抗菌性能得到增强,各种整理剂大分子能更充分的附着在织物表面。在试验手段方面,通过合适的浓度配比,调节合适的水浴温度和时间,结合最佳的浸轧技术,使得测试效果最佳,最适合人体。本发明方法工艺简单,成本低,安全环保,采用的整理剂均为改性整理剂,充分利用了整理剂改性后的突出优点弥补了丝绸织物本身的缺陷,可有效提高真丝织物的抗皱抗菌性能,并且对织物无任何损伤,使真丝织物保持原有的手感和韧性。The invention provides an anti-wrinkle and anti-bacterial treatment method for silk fabrics. Chitosan itself has obvious anti-bacterial effect, and the biocompatibility is further improved after modification. Secondly, the modified silicone finishing agent can be further easily produced The disadvantage of wrinkles is that the antibacterial properties of the fabric are enhanced after the oxygen-containing groups in graphene are combined with the fabric fibers, and various finishing agent macromolecules can be more fully attached to the fabric surface. In terms of test methods, through the appropriate concentration ratio, adjusting the appropriate water bath temperature and time, combined with the best padding technology, the test effect is the best and most suitable for the human body. The method of the invention has the advantages of simple process, low cost, safety and environmental protection. The finishing agents used are all modified finishing agents, which make full use of the outstanding advantages of the modified finishing agents to make up for the defects of silk fabrics, and can effectively improve the anti-wrinkle and antibacterial properties of silk fabrics. performance, without any damage to the fabric, so that the silk fabric maintains its original feel and toughness.
Description
技术领域technical field
本发明涉及一种织物,具体涉及一种真丝织物的处理方法。The invention relates to a fabric, in particular to a method for treating real silk fabrics.
背景技术Background technique
真丝织物是一种由天然桑蚕丝纤维制成的面料,平整光洁,色彩鲜艳纯正,手感柔软,外观轻盈,悬垂性好,且由于其穿着舒适、吸湿透气、原料来源于自然、对人体皮肤亲和力好,从古至今深受人们喜爱。Silk fabric is a kind of fabric made of natural mulberry silk fiber. It is flat and smooth, bright and pure in color, soft to the touch, light in appearance, and good in drapability. Well, it has been loved by people since ancient times.
真丝织物具有诸多优良性能,但其在漂洗过程中容易产生褶皱和收缩现象,这是它的典型缺点。随着近年来新型化学纤维的不断涌现,真丝织物的缺点愈显突出,所以改善其抗皱性能并赋予其多种特殊功能具有重要意义。另外,真丝中的天然纤维中含有大量纤维素和蛋白质,有利于细菌的生长和繁殖,因此很有必要对真丝织物进行抗菌处理,使其在穿着中更具安全保健作用。Silk fabric has many excellent properties, but it is prone to wrinkles and shrinkage during the rinsing process, which is its typical disadvantage. With the continuous emergence of new chemical fibers in recent years, the shortcomings of real silk fabrics have become more prominent, so it is of great significance to improve its anti-wrinkle performance and endow it with various special functions. In addition, the natural fibers in real silk contain a lot of cellulose and protein, which is conducive to the growth and reproduction of bacteria. Therefore, it is necessary to carry out antibacterial treatment on real silk fabrics to make them more safe and healthy during wearing.
发明内容Contents of the invention
发明目的:本发明的目的在于针对现有技术的不足,提供一种真丝织物的抗皱抗菌处理方法,采用该方法处理后的真丝织物,可有效提高抗皱抗菌性能,并且对织物无损伤,使其保持原有的手感和韧性。Purpose of the invention: the purpose of the present invention is to address the deficiencies in the prior art and provide a method for anti-wrinkle and antibacterial treatment of silk fabrics. The silk fabrics treated by this method can effectively improve the anti-wrinkle and antibacterial performance, and have no damage to the fabric, making it Maintain the original feel and toughness.
技术方案:本发明提供了一种真丝织物的抗皱抗菌处理方法,包括以下步骤:Technical solution: the invention provides a method for anti-wrinkle and antibacterial treatment of real silk fabrics, comprising the following steps:
(1)分别配制浓度为2~10g/L的改性有机硅整理剂水溶液和浓度为2~10g/L的MgCl2▪6H2O催化剂水溶液,将两种水溶液混合均匀,其中改性有机硅整理剂水溶液的体积浓度在30%~70%的范围;(1) Prepare the modified silicone finishing agent aqueous solution with a concentration of 2-10g/L and the MgCl 2 ▪6H 2 O catalyst aqueous solution with a concentration of 2-10g/L, mix the two aqueous solutions evenly, and the modified silicone The volume concentration of the finishing agent aqueous solution is in the range of 30%~70%;
(2)取步骤(1)100~200ml溶液于容器中,置于20~50℃的水浴环境下加热5min后放入真丝织物,使真丝织物完全浸没,并继续水浴加热5min;(2) Take 100-200ml of the solution from step (1) in a container, heat it in a water bath at 20-50°C for 5 minutes, put it into the silk fabric, completely submerge the silk fabric, and continue heating in the water bath for 5 minutes;
(3)取出真丝织物,在步骤(1)配制的溶液中二浸二轧,而后烘干,烘干温度110~130℃,烘干时间1~3min;(3) Take out the real silk fabric, dip and roll twice in the solution prepared in step (1), and then dry it at a temperature of 110-130°C and a drying time of 1-3 minutes;
(4)经烘干后的真丝织物在体积分数为2~10%的肥皂液中漂洗,温度30~50℃,时间20~50min后取出,清水洗净后烫干;(4) Rinse the dried silk fabric in a soap solution with a volume fraction of 2-10%, at a temperature of 30-50°C, for 20-50 minutes, take it out, wash it with clean water and iron it dry;
(5)以0.2mol/L乙酸溶液为溶剂配置质量分数0.1%~1%的改性壳聚糖溶液作为抗菌纳米整理剂;(5) Use 0.2mol/L acetic acid solution as a solvent to configure a modified chitosan solution with a mass fraction of 0.1% to 1% as an antibacterial nano-finishing agent;
(6)将步骤(4)中烫干后的真丝织物放入抗菌纳米整理剂中,并在50℃水浴锅内振荡40min;(6) Put the dried silk fabric in step (4) into the antibacterial nano-finishing agent, and shake it in a water bath at 50°C for 40 minutes;
(7)取出真丝织物,用去离子水洗净,将织物烘干;(7) Take out the silk fabric, wash it with deionized water, and dry the fabric;
(8)将烘干后的织物浸没于石墨烯分散液中2h后取出,然后再次进行二浸二轧操作,最后常温下鼓风吹干织物。(8) Immerse the dried fabric in the graphene dispersion solution for 2 hours, then take it out, then perform two dipping and two rolling operations again, and finally blow dry the fabric at room temperature.
进一步,步骤(1)所述改性有机硅整理剂采用聚醚基硅烷和氨基硅烷为主要原料,采用1:3的体积比,常温下通过乳液聚合法制成氨基改性的有机硅溶液。Further, the modified silicone finishing agent in step (1) uses polyether-based silane and aminosilane as main raw materials, and adopts a volume ratio of 1:3 to prepare an amino-modified silicone solution by emulsion polymerization at room temperature.
进一步,步骤(3)二浸二轧采用轧液率100%的三辊小轧车。Further, in step (3), the second dipping and the second rolling adopt a small three-roll rolling car with a liquid rolling rate of 100%.
进一步,步骤(5)所述改性壳聚糖溶液采用乙酸溶液与壳聚糖为主要原料,采用2:3的体积比,常温下反应得到改性的壳聚糖溶液。Further, the modified chitosan solution in step (5) adopts acetic acid solution and chitosan as main raw materials, adopts a volume ratio of 2:3, and reacts at normal temperature to obtain a modified chitosan solution.
进一步,步骤(6)水浴锅的振荡速率为100r/min。Further, in step (6), the oscillation rate of the water bath is 100r/min.
进一步,步骤(7)中的烘干温度为100℃~120℃,烘干时间为1min。Further, the drying temperature in step (7) is 100° C. to 120° C., and the drying time is 1 min.
进一步,步骤(8)中的石墨烯分散液是通过Hummers法制备,首先是氧化石墨烯的制备,用浓硫酸10~20ml、高锰酸钾4g、石墨1g混合均匀,在40℃~50℃温度下反应30min,加5ml~10ml 30%体积分数的双氧水,再用200ml~300ml的10%体积分数的稀盐酸洗涤,洗涤后在室温下鼓风干燥,得到氧化石墨烯;再将氧化石墨烯研磨成粉,微波下迅速加热到700℃~1000℃还原氧化石墨烯,然后将就加热后的粉末与水以质量比10:7的比例混合均匀即可。Further, the graphene dispersion in step (8) is prepared by the Hummers method. Firstly, the graphene oxide is prepared by mixing 10-20ml of concentrated sulfuric acid, 4g of potassium permanganate, and 1g of graphite. React at high temperature for 30 minutes, add 5ml~10ml of 30% volume fraction of hydrogen peroxide, then wash with 200ml~300ml of 10% volume fraction of dilute hydrochloric acid, after washing, blow dry at room temperature to obtain graphene oxide; Grind into powder, rapidly heat to 700°C~1000°C under microwave to reduce graphene oxide, and then mix the heated powder and water evenly at a mass ratio of 10:7.
发明原理:1、本发明使用的氨基改性有机硅整理剂中的活泼的硅羟基与纤维素中的羟基反应形成交联网状结构,达到抗皱效果,加入氨基后则有机硅的水溶性提高,有利于反应的充分进行。2、使用的改性壳聚糖整理剂能与细胞膜上的磷脂膜结合,导致膜蛋白变性,膜结构被破坏,达到抗菌效果,酰化后的壳聚糖生物相容性更佳。3、石墨烯纳米材料的融入到丝纤维中不仅能使织物抗菌效果更好,其本身的超强吸附大分子的能力更能使有机硅分子与壳聚糖分子更好地附着在织物上面。使得处理后的真丝织物即使在多次洗涤后仍然具有较好的抗菌抗皱效果。Principle of the invention: 1. The active silicon hydroxyl group in the amino-modified organosilicon finishing agent used in the present invention reacts with the hydroxyl group in the cellulose to form a cross-linked network structure to achieve the anti-wrinkle effect. After adding the amino group, the water solubility of the organosilicon increases. It is conducive to the full progress of the reaction. 2. The modified chitosan finishing agent used can combine with the phospholipid membrane on the cell membrane, resulting in denaturation of membrane protein, destruction of membrane structure, and antibacterial effect. The biocompatibility of chitosan after acylation is better. 3. The incorporation of graphene nanomaterials into silk fibers can not only make the antibacterial effect of the fabric better, but also make the organic silicon molecules and chitosan molecules better adhere to the fabric due to its super strong adsorption capacity of macromolecules. The treated silk fabric still has good antibacterial and anti-wrinkle effects even after repeated washing.
有益效果:壳聚糖本身具有明显的抗菌效果,生物相容性在改性后得到进一步提高,其次,改性后的有机硅整理剂可以进一步易产生褶皱的缺点,将石墨烯中的含氧集团与织物纤维结合之后织物抗菌性能得到增强,各种整理剂大分子能更充分的附着在织物表面。在试验手段方面,通过合适的浓度配比,调节合适的水浴温度和时间,结合最佳的浸轧技术,使得测试效果最佳,最适合人体。本发明方法工艺简单,成本低,安全环保,采用的整理剂均为改性整理剂,充分利用了整理剂改性后的突出优点弥补了丝绸织物本身的缺陷,可有效提高真丝织物的抗皱抗菌性能,并且对织物无任何损伤,使真丝织物保持原有的手感和韧性。Beneficial effects: chitosan itself has obvious antibacterial effect, and the biocompatibility is further improved after modification. Secondly, the modified silicone finishing agent can further easily produce wrinkles, and the oxygen in graphene After the group is combined with the fabric fiber, the antibacterial performance of the fabric is enhanced, and the macromolecules of various finishing agents can be more fully attached to the surface of the fabric. In terms of test methods, through the appropriate concentration ratio, adjusting the appropriate water bath temperature and time, combined with the best padding technology, the test effect is the best and most suitable for the human body. The method of the invention has the advantages of simple process, low cost, safety and environmental protection. The finishing agents used are all modified finishing agents, which make full use of the outstanding advantages of the modified finishing agents to make up for the defects of silk fabrics, and can effectively improve the anti-wrinkle and antibacterial properties of silk fabrics. performance, without any damage to the fabric, so that the silk fabric maintains its original feel and toughness.
具体实施方式Detailed ways
下面对本发明技术方案进行详细说明,但是本发明的保护范围不局限于所述实施例。The technical solutions of the present invention will be described in detail below, but the protection scope of the present invention is not limited to the embodiments.
实施例1:一种真丝织物的抗皱抗菌处理方法,包括以下步骤:Embodiment 1: a kind of anti-wrinkle antibacterial treatment method of real silk fabric, comprises the following steps:
第一步:将改性有机硅整理剂配置成浓度为3g/L的水溶液,按2:1的体积比加入浓度为6g/L的MgCl2▪6H2O催化剂水溶液,混合均匀;The first step: configure the modified silicone finishing agent into an aqueous solution with a concentration of 3g/L, add an aqueous solution of MgCl2 6H2O catalyst with a concentration of 6g/L at a volume ratio of 2:1, and mix well;
第二步:取上述部分溶液于烧杯中,置于30℃的水浴环境下进行加热5min后放入真丝织物,继续水浴5min;Step 2: Take the above part of the solution in a beaker, place it in a water bath at 30°C for 5 minutes, put it into silk fabric, and continue the water bath for 5 minutes;
第三步:取出真丝织物,使用第一步中配置溶液对织物进行浸染,然后使用实验室三辊小轧车(轧液率100%)对浸染后的织物进行二浸二轧,然后进行烘干,其中烘干温度130℃,烘干时间3min;The third step: take out the real silk fabric, use the configuration solution in the first step to dip-dye the fabric, and then use the laboratory three-roller small padding machine (rolling liquid rate 100%) to perform two-dipping and two-rolling on the dip-dyed fabric, and then dry it Drying, where the drying temperature is 130°C and the drying time is 3 minutes;
第四步:经烘干后的织物在5%肥皂液中40℃恒温水浴中漂洗30min后取出,清水洗若干次后烫干;Step 4: Rinse the dried fabric in 5% soap solution in a 40°C constant temperature water bath for 30 minutes, take it out, wash it several times with water, and iron it dry;
第五步:以0.2mol/L乙酸溶液为溶剂配置质量分数0.6%的改性壳聚糖溶液作为抗菌纳米整理剂,通过试验发现大肠杆菌和金黄色葡萄球菌在0.6%的改性壳聚糖中需要50h-60h内才能达到生长顶点,而不含改性壳聚糖的溶液再24h内便可达到生长顶峰;Step 5: Use 0.2mol/L acetic acid solution as a solvent to configure a modified chitosan solution with a mass fraction of 0.6% as an antibacterial nano-finishing agent. Through experiments, it was found that Escherichia coli and Staphylococcus aureus in 0.6% modified chitosan It takes 50h-60h to reach the growth peak, while the solution without modified chitosan can reach the growth peak within 24h;
第六步:取壳聚糖溶液于烧杯中,将第四步中烫干后的真丝织物放入其中,并在50℃水浴锅内振荡40min,其中水浴锅的振荡速率为100r/min;Step 6: Put the chitosan solution in a beaker, put the dried silk fabric in the fourth step into it, and vibrate in a water bath at 50°C for 40 minutes, wherein the oscillation speed of the water bath is 100r/min;
第七步:取出织物,去离子水清洗若干次,取最后一次清洗液测定PH值,若为中性则表示乙酸已洗净,将织物烘干,烘干温度为100℃~120℃,烘干时间1min;Step 7: Take out the fabric, wash it several times with deionized water, take the last cleaning solution to measure the pH value, if it is neutral, it means that the acetic acid has been washed, dry the fabric at 100°C~120°C, Drying time 1min;
第八步:将烘干后的织物浸没于氧化石墨烯分散液中2h后取出,然后通过二浸二轧操作使石墨烯中的含氧集团与丝纤维结合的更稳固,最后常温下鼓风吹干织物;Step 8: Submerge the dried fabric in the graphene oxide dispersion for 2 hours, then take it out, and then make the oxygen-containing group in the graphene and the silk fiber more stable through two dipping and two rolling operations, and finally blast at room temperature blow dry the fabric;
第九步:通过扫描电镜观察织物表面分子的附着情况,发现与清洗前相比,总体的大分子的附着量只减少了5%,保持了95%以上的附着量。Step 9: Observing the adhesion of molecules on the surface of the fabric through scanning electron microscopy, it is found that compared with before washing, the overall adhesion of macromolecules is only reduced by 5%, and more than 95% of the adhesion is maintained.
实施例2:一种真丝织物的抗皱抗菌处理方法,包括以下步骤:Embodiment 2: a kind of anti-wrinkle antibacterial treatment method of real silk fabric, comprises the following steps:
第一步:将改性有机硅整理剂配置成浓度为6g/L的水溶液,按1:1体积比加入浓度为6g/L的MgCl2▪6H2O催化剂水溶液,混合均匀;The first step: configure the modified silicone finishing agent into an aqueous solution with a concentration of 6g/L, add MgCl2 6H2O catalyst aqueous solution with a concentration of 6g/L at a volume ratio of 1:1, and mix well;
第二步:取上述部分溶液于烧杯中,置于30℃的水浴环境下进行加热5min后放入真丝织物,继续水浴5min;Step 2: Take the above part of the solution in a beaker, place it in a water bath at 30°C for 5 minutes, put it into silk fabric, and continue the water bath for 5 minutes;
第三步:取出真丝织物,使用第一步中配置溶液对织物进行浸染,然后使用实验室三辊小轧车(轧液率100%)对浸染后的织物进行二浸二轧,然后进行烘干,其中烘干温度130℃,烘干时间3min;The third step: take out the real silk fabric, use the configuration solution in the first step to dip-dye the fabric, and then use the laboratory three-roller small padding machine (rolling liquid rate 100%) to perform two-dipping and two-rolling on the dip-dyed fabric, and then dry it Drying, where the drying temperature is 130°C and the drying time is 3 minutes;
第四步:经烘干后的织物在5%肥皂液中40℃恒温水浴中漂洗30min后取出,清水洗若干次后烫干;Step 4: Rinse the dried fabric in 5% soap solution in a 40°C constant temperature water bath for 30 minutes, take it out, wash it several times with water, and iron it dry;
第五步:以0.2mol/L乙酸溶液为溶剂配置质量分数0.6%的改性壳聚糖溶液作为抗菌纳米整理剂,通过试验发现大肠杆菌和金黄色葡萄球菌在0.6%的改性壳聚糖中需要50h-60h内才能达到生长顶点,而不含改性壳聚糖的溶液再24h内便可达到生长顶峰;Step 5: Use 0.2mol/L acetic acid solution as a solvent to configure a modified chitosan solution with a mass fraction of 0.6% as an antibacterial nano-finishing agent. Through experiments, it was found that Escherichia coli and Staphylococcus aureus in 0.6% modified chitosan It takes 50h-60h to reach the growth peak, while the solution without modified chitosan can reach the growth peak within 24h;
第六步:取壳聚糖溶液于烧杯中,将第四步中烫干后的真丝织物放入其中,并在50℃水浴锅内振荡40min,其中水浴锅的振荡速率为100r/min;Step 6: Put the chitosan solution in a beaker, put the dried silk fabric in the fourth step into it, and vibrate in a water bath at 50°C for 40 minutes, wherein the oscillation speed of the water bath is 100r/min;
第七步:取出织物,去离子水清洗若干次,取最后一次清洗液测定PH值,若为中性则表示乙酸已洗净,将织物烘干,烘干温度为100℃~120℃,烘干时间1min;Step 7: Take out the fabric, wash it several times with deionized water, take the last cleaning solution to measure the pH value, if it is neutral, it means that the acetic acid has been washed, dry the fabric at 100°C~120°C, Drying time 1min;
第八步:将烘干后的织物浸没于氧化石墨烯分散液中2h后取出,使石墨烯中的含氧基团与真丝纤维结合的更稳固;Step 8: Immerse the dried fabric in the graphene oxide dispersion for 2 hours and take it out, so that the oxygen-containing groups in the graphene can be more firmly combined with the silk fiber;
第九步:通过扫描电镜观察织物表面分子的附着情况,发现与清洗前相比,总体的大分子的附着量减少了10%,保持了90%以上的附着量。Step 9: Observing the adhesion of molecules on the surface of the fabric through a scanning electron microscope, it is found that compared with before washing, the overall adhesion of macromolecules has decreased by 10%, and more than 90% of the adhesion has been maintained.
实施例3:一种真丝织物的抗皱抗菌处理方法,包括以下步骤:Embodiment 3: a kind of anti-wrinkle antibacterial treatment method of real silk fabric, comprises the following steps:
第一步:将改性有机硅整理剂配置成浓度为6g/L的水溶液,按1:2的体积比加入浓度为9g/L的MgCl2▪6H2O催化剂水溶液,混合均匀;The first step: configure the modified silicone finishing agent into an aqueous solution with a concentration of 6g/L, add MgCl2 6H2O catalyst aqueous solution with a concentration of 9g/L at a volume ratio of 1:2, and mix well;
第二步:取上述部分溶液于烧杯中,置于30℃的水浴环境下进行加热5min后放入真丝织物,继续水浴5min;Step 2: Take the above part of the solution in a beaker, place it in a water bath at 30°C for 5 minutes, put it into silk fabric, and continue the water bath for 5 minutes;
第三步:取出真丝织物,使用第一步中配置溶液对织物进行浸染,然后使用实验室三辊小轧车(轧液率100%)对浸染后的织物进行二浸二轧,然后进行烘干,其中烘干温度130℃,烘干时间3min;The third step: take out the real silk fabric, use the configuration solution in the first step to dip-dye the fabric, and then use the laboratory three-roller small padding machine (rolling liquid rate 100%) to perform two-dipping and two-rolling on the dip-dyed fabric, and then dry it Drying, where the drying temperature is 130°C and the drying time is 3 minutes;
第四步:经烘干后的织物在5%肥皂液中40℃恒温水浴中漂洗30min后取出,清水洗若干次后烫干;Step 4: Rinse the dried fabric in 5% soap solution in a 40°C constant temperature water bath for 30 minutes, take it out, wash it several times with water, and iron it dry;
第五步:以0.2mol/L乙酸溶液为溶剂配置质量分数0.6%的改性壳聚糖溶液作为抗菌纳米整理剂,通过试验发现大肠杆菌和金黄色葡萄球菌在0.6%的改性壳聚糖中需要50h-60h内才能达到生长顶点,而不含改性壳聚糖的溶液再24h内便可达到生长顶峰;Step 5: Use 0.2mol/L acetic acid solution as a solvent to configure a modified chitosan solution with a mass fraction of 0.6% as an antibacterial nano-finishing agent. Through experiments, it was found that Escherichia coli and Staphylococcus aureus in 0.6% modified chitosan It takes 50h-60h to reach the growth peak, while the solution without modified chitosan can reach the growth peak within 24h;
第六步:取壳聚糖溶液于烧杯中,将第四步中烫干后的真丝织物放入其中,并在50℃水浴锅内振荡40min,其中水浴锅的振荡速率为100r/min;Step 6: Put the chitosan solution in a beaker, put the dried silk fabric in the fourth step into it, and vibrate in a water bath at 50°C for 40 minutes, wherein the oscillation speed of the water bath is 100r/min;
第七步:取出织物,去离子水清洗若干次,取最后一次清洗液测定PH值,若为中性则表示乙酸已洗净,将织物烘干,烘干温度为100℃~120℃,烘干时间1min。。第八步:将烘干后的织物浸没于氧化石墨烯分散液中2h后取出,然后在700℃~1000℃的高温下烘干使氧化石墨烯得到还原,使石墨烯中的含氧集团与真丝纤维结合的更稳固;Step 7: Take out the fabric, wash it several times with deionized water, take the last cleaning solution to measure the pH value, if it is neutral, it means that the acetic acid has been washed, dry the fabric at 100°C~120°C, Drying time 1min. . Step 8: Immerse the dried fabric in the graphene oxide dispersion liquid for 2 hours, then take it out, and then dry it at a high temperature of 700°C~1000°C to reduce the graphene oxide, so that the oxygen-containing groups in the graphene and The combination of silk fibers is more stable;
第九步:通过扫描电镜观察织物表面分子的附着情况,发现与清洗前相比,总体的大分子的附着量只减少了8%,保持了92%以上的附着量。Step 9: Observing the adhesion of molecules on the surface of the fabric through a scanning electron microscope, it was found that compared with before washing, the overall adhesion of macromolecules was only reduced by 8%, and more than 92% of the adhesion was maintained.
Claims (7)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810192484.2A CN108342904A (en) | 2018-03-09 | 2018-03-09 | A kind of creasing anti-bacterial processing method of real silk fabric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810192484.2A CN108342904A (en) | 2018-03-09 | 2018-03-09 | A kind of creasing anti-bacterial processing method of real silk fabric |
Publications (1)
Publication Number | Publication Date |
---|---|
CN108342904A true CN108342904A (en) | 2018-07-31 |
Family
ID=62957501
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201810192484.2A Pending CN108342904A (en) | 2018-03-09 | 2018-03-09 | A kind of creasing anti-bacterial processing method of real silk fabric |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN108342904A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109487555A (en) * | 2018-12-02 | 2019-03-19 | 南京林业大学 | The modified antibiotic fabric preparation method of graphene/chitosan binary synergistic |
CN110284332A (en) * | 2019-07-29 | 2019-09-27 | 苏州经贸职业技术学院 | A kind of real silk crease-proof antibacterial finish agent and preparation method thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001207381A (en) * | 2000-12-20 | 2001-08-03 | Nakamura Kenji | Composition for fiber treatment |
CN105862393A (en) * | 2016-04-12 | 2016-08-17 | 西南大学 | Production method of antibacterial sericin-containing silk/graphene film |
CN107287905A (en) * | 2017-06-26 | 2017-10-24 | 苏州威尔德工贸有限公司 | A kind of silk fabric creasing anti-bacterial method for sorting |
-
2018
- 2018-03-09 CN CN201810192484.2A patent/CN108342904A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001207381A (en) * | 2000-12-20 | 2001-08-03 | Nakamura Kenji | Composition for fiber treatment |
CN105862393A (en) * | 2016-04-12 | 2016-08-17 | 西南大学 | Production method of antibacterial sericin-containing silk/graphene film |
CN107287905A (en) * | 2017-06-26 | 2017-10-24 | 苏州威尔德工贸有限公司 | A kind of silk fabric creasing anti-bacterial method for sorting |
Non-Patent Citations (3)
Title |
---|
姚静等: "壳聚糖有机硅微乳液整理真丝绸的特性研究", 《丝绸》 * |
孙理: ""壳聚糖对真丝绸的抗皱抗菌整理与特性研究"", 《中国优秀博硕士学位论文全文数据库(硕士)工程科技I辑》 * |
王建明等: "真丝织物的有机硅防皱整理", 《北京服装学院学报(自然科学版)》 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109487555A (en) * | 2018-12-02 | 2019-03-19 | 南京林业大学 | The modified antibiotic fabric preparation method of graphene/chitosan binary synergistic |
CN110284332A (en) * | 2019-07-29 | 2019-09-27 | 苏州经贸职业技术学院 | A kind of real silk crease-proof antibacterial finish agent and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104878591B (en) | A kind of super-hydrophobic, method for sorting of hydrophilic two-sided different in nature bafta | |
CN104562658A (en) | Amino acid nano-silver modified finishing agent as well as preparation method of finishing agent and modified fishing shell fabric | |
CN113481728A (en) | Silk fibroin nano-silver antibacterial color developing finishing agent and preparation method and application thereof | |
CN104790203B (en) | A kind of selfreparing, the method for sorting of hydrophobic bafta | |
CN104264232A (en) | Preparation method of functional bast fiber through degumming and modification | |
CN111996815A (en) | Preparation and dyeing of boron/silicon-containing hybrid functional protein fiber | |
CN108342904A (en) | A kind of creasing anti-bacterial processing method of real silk fabric | |
CN107675480A (en) | A kind of method that directional water guiding fabric is obtained using corona treatment | |
WO2022012012A1 (en) | Strongly hydrophobic real silk fabric and preparation method therefor | |
CN107700203A (en) | A kind of processing method of modified soybean fiber | |
CN115652613B (en) | Silver ion antibacterial fabric and production method thereof | |
CN104746266A (en) | Anion health care finishing technology of all cotton jacquard fabric | |
CN112127153A (en) | Antibacterial and deodorant textile and preparation method thereof | |
CN114734689A (en) | Fabric based on zinc ion antibacterial and heating and weaving method thereof | |
CN112941907A (en) | MXene two-dimensional nanosheet-based multifunctional real silk fabric and preparation method thereof | |
CN113652870A (en) | Preparation method of multifunctional fibroin finishing agent and application of multifunctional fibroin finishing agent to polyester fabric | |
CN112144276A (en) | Preparation method of anti-ultraviolet cotton fabric | |
CN111139641A (en) | Preparation method of wool tops capable of being comprehensively and easily nursed and product of wool tops | |
CN105951421A (en) | Preparation method of soy protein modified lotus fiber fabric | |
CN104790201B (en) | A kind of endowing terylene fabric high-hydrophilic and can reactive group nitrification method of reducing | |
CN104313871A (en) | Preparation method of lyophobic nano fiber fabric | |
CN114687201B (en) | Preparation method of honeysuckle dyed antibacterial textile and product thereof | |
CN110344267B (en) | A kind of preparation method of easy-dyeing-fixing-soap-resistant fabric based on reactive dyeing | |
CN103789863A (en) | Manufacturing method of white acrylic conductive fiber | |
CN108252105A (en) | A kind of surface treatment method of glass fabric |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20180731 |
|
RJ01 | Rejection of invention patent application after publication |