CN104790055B - A kind of preparation method of viscose fiber containing grass coral extract - Google Patents
A kind of preparation method of viscose fiber containing grass coral extract Download PDFInfo
- Publication number
- CN104790055B CN104790055B CN201510176510.9A CN201510176510A CN104790055B CN 104790055 B CN104790055 B CN 104790055B CN 201510176510 A CN201510176510 A CN 201510176510A CN 104790055 B CN104790055 B CN 104790055B
- Authority
- CN
- China
- Prior art keywords
- preparation
- viscose
- dispersant
- liquid
- herba pileae
- 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.)
- Active
Links
- 229920000297 Rayon Polymers 0.000 title claims abstract description 42
- 239000000835 fiber Substances 0.000 title claims abstract description 36
- 239000000284 extract Substances 0.000 title claims abstract description 29
- 238000002360 preparation method Methods 0.000 title claims abstract description 29
- 244000132059 Carica parviflora Species 0.000 title description 16
- 235000014653 Carica parviflora Nutrition 0.000 title description 12
- 244000025254 Cannabis sativa Species 0.000 title description 10
- 238000009987 spinning Methods 0.000 claims abstract description 43
- 239000002270 dispersing agent Substances 0.000 claims abstract description 40
- 230000000844 anti-bacterial effect Effects 0.000 claims abstract description 25
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 claims abstract description 23
- 239000001768 carboxy methyl cellulose Substances 0.000 claims abstract description 13
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 claims abstract description 13
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 claims abstract description 13
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 7
- 238000012805 post-processing Methods 0.000 claims abstract description 7
- 241000222122 Candida albicans Species 0.000 claims abstract description 5
- 241000191967 Staphylococcus aureus Species 0.000 claims abstract description 5
- 229940095731 candida albicans Drugs 0.000 claims abstract description 5
- 230000000845 anti-microbial effect Effects 0.000 claims abstract 6
- 239000007788 liquid Substances 0.000 claims description 49
- 238000003756 stirring Methods 0.000 claims description 14
- 239000000843 powder Substances 0.000 claims description 13
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 238000002156 mixing Methods 0.000 claims description 9
- -1 sulfoalkyl ester Chemical class 0.000 claims description 9
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 6
- 229910052938 sodium sulfate Inorganic materials 0.000 claims description 6
- 235000011152 sodium sulphate Nutrition 0.000 claims description 6
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 claims description 6
- 229960001763 zinc sulfate Drugs 0.000 claims description 6
- 229910000368 zinc sulfate Inorganic materials 0.000 claims description 6
- ZROGCCBNZBKLEL-FHXNIQKESA-N Astilbin Natural products O([C@H]1[C@@H](c2cc(O)c(O)cc2)Oc2c(c(O)cc(O)c2)C1=O)[C@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](C)O1 ZROGCCBNZBKLEL-FHXNIQKESA-N 0.000 claims description 3
- ZROGCCBNZBKLEL-MPRHSVQHSA-N astilbin Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1O[C@H]1C(=O)C2=C(O)C=C(O)C=C2O[C@@H]1C1=CC=C(O)C(O)=C1 ZROGCCBNZBKLEL-MPRHSVQHSA-N 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 2
- 229920002678 cellulose Polymers 0.000 claims description 2
- 239000001913 cellulose Substances 0.000 claims description 2
- 230000032050 esterification Effects 0.000 claims description 2
- 238000005886 esterification reaction Methods 0.000 claims description 2
- 230000001112 coagulating effect Effects 0.000 claims 2
- HOEVRHHMDJKUMZ-UHFFFAOYSA-N Isofraxidin Chemical compound C1=CC(=O)OC2=C1C=C(OC)C(O)=C2OC HOEVRHHMDJKUMZ-UHFFFAOYSA-N 0.000 claims 1
- ANCHXLMTFNOVDK-UHFFFAOYSA-N Isofraxidin Natural products COC1=C(O)C(OC)=CC2=C1OC=CC2=O ANCHXLMTFNOVDK-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000003242 anti bacterial agent Substances 0.000 description 20
- 239000000243 solution Substances 0.000 description 16
- 239000011550 stock solution Substances 0.000 description 14
- 229920003123 carboxymethyl cellulose sodium Polymers 0.000 description 10
- 229940063834 carboxymethylcellulose sodium Drugs 0.000 description 10
- 230000015271 coagulation Effects 0.000 description 10
- 238000005345 coagulation Methods 0.000 description 10
- 238000002474 experimental method Methods 0.000 description 10
- 238000000556 factor analysis Methods 0.000 description 10
- 230000005764 inhibitory process Effects 0.000 description 9
- 235000014113 dietary fatty acids Nutrition 0.000 description 8
- 239000000194 fatty acid Substances 0.000 description 8
- 229930195729 fatty acid Natural products 0.000 description 8
- 238000011056 performance test Methods 0.000 description 7
- 238000001035 drying Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000004753 textile Substances 0.000 description 6
- 238000005406 washing Methods 0.000 description 5
- 238000006477 desulfuration reaction Methods 0.000 description 4
- 230000023556 desulfurization Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000036541 health Effects 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 3
- 241000588724 Escherichia coli Species 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 206010059866 Drug resistance Diseases 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Artificial Filaments (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
技术领域 technical field
本发明属于人造纤维制造技术领域,涉及一种纤维的制备方法,具体涉及一种含草珊瑚提取物的粘胶纤维的制备方法。 The invention belongs to the technical field of man-made fibers, and relates to a method for preparing fibers, in particular to a method for preparing viscose fibers containing coral extracts.
背景技术 Background technique
现有的常规粘胶纤维为再生纤维素纤维,其制品具有吸湿透气性好,穿着舒适的特点。随着人们生活水平的提高和生活观念的改变,人们对纺织品的保健功能越来越重视,希望现有的粘胶纤维纺织品在抗菌性能等方面得到改善;且现有的抗菌粘胶纤维制品存在抗菌能力不足、强度不高、染色效果较差、湿模量较低造成织物尺寸不稳定等缺陷。 Existing conventional viscose fiber is regenerated cellulose fiber, and its products have the characteristics of good moisture absorption and air permeability, and comfortable wearing. With the improvement of people's living standards and the change of life concepts, people pay more and more attention to the health care function of textiles, and hope that the existing viscose fiber textiles can be improved in terms of antibacterial properties; Insufficient antibacterial ability, low strength, poor dyeing effect, low wet modulus, resulting in unstable fabric size and other defects.
抗菌纤维制品所使用的抗菌剂基本分为三大类,即天然抗菌剂、有机抗菌剂和无机抗菌剂。有机抗菌剂抑菌杀菌迅速、高效,但对人体有副作用,细菌易产生耐药性,且时效性差、不耐高温;无机类抗菌剂主要为具有抗菌作用的金属无机盐及抗菌沸石。此类抗菌剂中的重金属离子,极易通过与人体皮肤接触被人体吸收,对人体的健康造成很大的潜在危害;天然抗菌剂具有抗菌高效,对人体安全,细菌不产生耐药性,且绿色环保等优点,因此,在应用中日益受到人们的重视。 The antibacterial agents used in antibacterial fiber products are basically divided into three categories, namely natural antibacterial agents, organic antibacterial agents and inorganic antibacterial agents. Organic antibacterial agents are quick and effective in inhibiting and killing bacteria, but they have side effects on the human body. Bacteria are prone to drug resistance, have poor timeliness, and are not resistant to high temperatures. Inorganic antibacterial agents are mainly metal inorganic salts and antibacterial zeolites with antibacterial effects. The heavy metal ions in such antibacterial agents are easily absorbed by the human body through contact with human skin, causing great potential harm to human health; natural antibacterial agents have high antibacterial efficiency, are safe for the human body, and bacteria do not produce drug resistance, and Environmental protection and other advantages, therefore, in the application of people's attention.
发明内容 Contents of the invention
本发明针对以上不足,提供一种含草珊瑚提取物的粘胶纤维的制备方法,实现以下发明目的: The present invention is aimed at above deficiency, provides a kind of preparation method of the viscose fiber containing grass coral extract, realizes following invention purpose:
(1)本发明制备的粘胶纤维抗菌能力强:对金黄色葡萄球菌的抑制率达99.1%-99.4%,对大肠杆菌的抑制率达98.7-99.2%,对白色念珠菌的抑制率达93.4-95.6%; (1) The viscose fiber prepared by the present invention has strong antibacterial ability: the inhibition rate to Staphylococcus aureus reaches 99.1%-99.4%, the inhibition rate to Escherichia coli reaches 98.7-99.2%, and the inhibition rate to Candida albicans reaches 93.4% -95.6%;
(2)本发明制备的粘胶纤维强度高,湿模量高:干态强度达6.2-6.3cN/dtex,湿态强度达4.7-4.9cN/dtex,断裂伸长率达23-25%,湿模量达0.63-0.65cN/dtex; (2) The viscose fiber prepared by the present invention has high strength and high wet modulus: the dry strength reaches 6.2-6.3cN/dtex, the wet strength reaches 4.7-4.9cN/dtex, and the elongation at break reaches 23-25%. The wet modulus reaches 0.63-0.65cN/dtex;
(3)本发明制备的粘胶纤维安全、环保、染色效果好,可代替化学染料的使用,避免对皮肤产生危害,有利于人们健康。 (3) The viscose fiber prepared by the invention is safe, environmentally friendly and has good dyeing effect, can replace the use of chemical dyes, avoid harm to the skin, and is beneficial to people's health.
为解决上述技术问题,采用以下技术方案: In order to solve the above technical problems, the following technical solutions are adopted:
一种含草珊瑚提取物的粘胶纤维的制备方法,包括以下步骤:抗菌剂溶液的制备,加入分散剂,加入羧甲基纤维素钠,和纺丝原液共混,纺丝,后处理; A method for preparing viscose fiber containing coral coral extract, comprising the following steps: preparing an antibacterial agent solution, adding a dispersant, adding sodium carboxymethyl cellulose, blending with spinning stock solution, spinning, and post-processing;
所述的加入分散剂步骤,加入的分散剂为脂肪酸磺烷基酯,分散剂占抗菌溶液的质量百分比为1.5%-2%。 In the step of adding a dispersant, the added dispersant is fatty acid sulfoalkyl ester, and the mass percentage of the dispersant in the antibacterial solution is 1.5%-2%.
以下是对上述技术方案的进一步改进: Following is the further improvement to above-mentioned technical scheme:
所述的抗菌剂溶液的制备步骤,将草珊瑚提取物粉末加入到温度为25±1℃的水中,加入量为100g/1000ml水,充分搅拌至粉末完全溶解制成抗菌剂溶液A,加入分散剂后制得溶液B。所述的加入分散剂步骤,加入的分散剂为脂肪酸磺烷基酯,分散剂占抗菌溶液的质量百分比为1.5%-2%。 The preparation step of the antibacterial agent solution is to add the powdered coral coral extract to water at a temperature of 25±1°C, the amount of addition is 100g/1000ml of water, stir well until the powder is completely dissolved to form an antibacterial agent solution A, add and disperse Solution B was prepared after dosing. In the step of adding a dispersant, the added dispersant is fatty acid sulfoalkyl ester, and the mass percentage of the dispersant in the antibacterial solution is 1.5%-2%.
所述的草珊瑚提取物粉末,技术指标为:干燥失重≦5.0%,重金属含量≦20ppm,异秦皮啶含量≥0.15mg/g,落新妇苷含量≥50mg/g,目数为80-120。 The technical indicators of the grass coral extract powder are: loss on drying≦5.0%, heavy metal content≦20ppm, isoferidin content≧0.15mg/g, astilbin content≧50mg/g, mesh number 80-120.
所述的和纺丝原液共混步骤,纺丝原液中纤维素质量百分含量为8-10%,NaOH质量百分含量为10-12%,熟成度10%NH4Cl值为39-40mL,酯化度为66-70%,碱纤比为1.0-1.2。 In the step of blending with the spinning stock solution, the mass percentage of cellulose in the spinning stock solution is 8-10%, the mass percentage of NaOH is 10-12%, and the NH 4 Cl value of 10% maturity is 39-40mL , the degree of esterification is 66-70%, and the ratio of alkali to fiber is 1.0-1.2.
所述的加入羧甲基纤维素钠步骤,将羧甲基纤维素钠粉按质量比为1:50-60的比例,在50~60℃的温度范围内,边搅拌边加入上述B液中,得C液。 In the step of adding sodium carboxymethyl cellulose, the sodium carboxymethyl cellulose powder is added into the above liquid B while stirring at a temperature range of 50-60°C in a mass ratio of 1:50-60 , to obtain liquid C.
所述的和纺丝原液共混步骤,将上述C液,按照纺丝原液15%-17%的质量比例,添加到纺丝原液中,搅拌分散后静置真空排泡,得D液。 In the step of blending with the spinning stock solution, the above-mentioned liquid C is added to the spinning stock solution at a mass ratio of 15%-17% of the spinning stock solution, stirred and dispersed, and left to stand for vacuum defoaming to obtain D liquid.
所述的纺丝步骤,凝固浴的温度10-14℃;所述的凝固浴由20-25g/L硫酸,35-38g/L硫酸钠和10-15g/L硫酸锌组成,纺丝速度为15-40m/min。 In the spinning step, the temperature of the coagulation bath is 10-14°C; the coagulation bath is composed of 20-25g/L sulfuric acid, 35-38g/L sodium sulfate and 10-15g/L zinc sulfate, and the spinning speed is 15-40m/min.
所述的纺丝速度优选为15-18m/min。 The spinning speed is preferably 15-18m/min.
所述的抗菌粘胶纤维,抗菌性能为:对金黄色葡萄球菌的抑制率为99.1%-99.4%,对大肠杆菌的抑制率为98.7-99.2%,对白色念珠菌的抑制率为93.4-95.6%。 The antibacterial viscose fiber has antibacterial properties: the inhibition rate to Staphylococcus aureus is 99.1%-99.4%, the inhibition rate to Escherichia coli is 98.7-99.2%, and the inhibition rate to Candida albicans is 93.4-95.6% %.
所述的抗菌粘胶纤维,技术性能指标为:干态强度为6.2-6.3cN/dtex,湿态强度为4.7-4.9cN/dtex,断裂伸长率为23-25%,湿模量为0.63-0.65cN/dtex。 The technical performance index of the antibacterial viscose fiber is as follows: the dry strength is 6.2-6.3cN/dtex, the wet strength is 4.7-4.9cN/dtex, the elongation at break is 23-25%, and the wet modulus is 0.63 -0.65cN/dtex.
本发明与现有技术相比,具有以下有益效果: Compared with the prior art, the present invention has the following beneficial effects:
(1)本发明制备的粘胶纤维抗菌能力强,对金黄色葡萄球菌的抑制率为99.1%-99.4%,对大肠杆菌的抑制率为98.7-99.2%,对白色念珠菌的抑制率为93.4-95.6%; (1) The viscose fiber prepared by the present invention has strong antibacterial ability, the inhibition rate to Staphylococcus aureus is 99.1%-99.4%, the inhibition rate to Escherichia coli is 98.7-99.2%, and the inhibition rate to Candida albicans is 93.4% -95.6%;
(2)本发明制备的粘胶纤维强度高,湿膜量高:干态强度为6.2-6.3cN/dtex,湿态强度为4.7-4.9cN/dtex,断裂伸长率为23-25%,湿模量为0.63-0.65cN/dtex; (2) The viscose fiber prepared by the present invention has high strength and high wet film content: the dry strength is 6.2-6.3cN/dtex, the wet strength is 4.7-4.9cN/dtex, and the elongation at break is 23-25%. The wet modulus is 0.63-0.65cN/dtex;
(3)本发明制备方法纺丝时抗菌剂流失小,制得的粘胶纤维抗菌性强且持久,经20次洗涤后仍具有良好的抗菌效果。 (3) The antibacterial agent lost during spinning by the preparation method of the present invention is small, and the prepared viscose fiber has strong and long-lasting antibacterial properties, and still has a good antibacterial effect after 20 times of washing.
(4)本发明制备的粘胶纤维安全、环保、染色效果好,可代替化学染料的使用,避免对皮肤产生危害,有利于人们健康。 (4) The viscose fiber prepared by the invention is safe, environmentally friendly and has good dyeing effect, can replace the use of chemical dyes, avoid harm to the skin, and is beneficial to people's health.
具体实施方式 detailed description
实施例1草珊瑚提取物原料Embodiment 1 Grass coral extract raw material
本发明选用的草珊瑚提取物原料为草珊瑚提取物粉末,原料的要求如下: The grass coral extract raw material that the present invention selects is grass coral extract powder, and the requirement of raw material is as follows:
干燥失重≦5.0%,重金属含量≦20ppm,异秦皮啶含量≥0.15mg/g,落新妇苷含量≥50mg/g,目数为80-120。 Loss on drying ≦5.0%, heavy metal content ≦20ppm, isoferidine content ≥0.15mg/g, astilbin content ≥50mg/g, mesh number 80-120.
实施例2Example 2
一种含草珊瑚提取物的粘胶纤维的制备方法,包括以下步骤: A preparation method of viscose fiber containing a grass coral extract, comprising the following steps:
(1)抗菌剂溶液的制备 (1) Preparation of antibacterial agent solution
将草珊瑚提取物粉末加入到温度为25±1℃的水中,加入量为100g/1000ml水,充分搅拌至粉末完全溶解制成抗菌剂溶液,得A液。 Add the powdered coral coral extract to water at a temperature of 25±1°C in an amount of 100g/1000ml of water, stir well until the powder is completely dissolved to form an antibacterial agent solution, and obtain liquid A.
(2)加入分散剂 (2) Add dispersant
向上述A液中加入分散剂,搅拌,得B液。 Add the dispersant to the above liquid A and stir to obtain liquid B.
(3)加入羧甲基纤维素钠 (3) Add carboxymethyl cellulose sodium
将羧甲基纤维素钠粉按一定的质量比,在50~60℃的温度范围内,边搅拌边加入上述B液中,得C液。 Add carboxymethyl cellulose sodium powder into the above liquid B while stirring in a temperature range of 50-60°C in a certain mass ratio to obtain liquid C.
(4)和纺丝原液共混 (4) Blending with spinning dope
将上述C液,按照纺丝原液15%的质量比,添加到纺丝原液中,搅拌分散后静置真空排泡,得D液。 The above liquid C was added to the spinning stock solution at a mass ratio of 15% of the spinning stock solution, stirred and dispersed, and then left to stand for vacuum defoaming to obtain liquid D.
(5)纺丝 (5) spinning
上述D液经计量泵计量后经烛形滤器和喷丝头进入12℃凝固浴;所述的凝固浴由25g/L硫酸,38g/L硫酸钠和15g/L硫酸锌组成,纺丝速度为16m/min。 Above-mentioned D liquid enters 12 ℃ of coagulation baths through candle filter and spinneret after metering pump metering; Described coagulation bath is made up of 25g/L sulfuric acid, 38g/L sodium sulfate and 15g/L zinc sulfate, and spinning speed is 16m/min.
(6)后处理 (6) Post-processing
经过脱硫、水洗、上油、烘干工序,制得本发明产品。 After desulfurization, water washing, oiling and drying processes, the product of the present invention is obtained.
实施例3分散剂种类单因素分析实验Embodiment 3 dispersant type single factor analysis experiment
采用实施例4-8所述的分散剂,分散剂的添加量占A液的质量比例均为1.5%,羧甲基纤维素钠和B液的质量比例均为1:50,按照实施2的制备方法制备含有草珊瑚提取物的粘胶纤维。 Adopt the dispersant described in embodiment 4-8, the mass ratio that the addition amount of dispersant accounts for A liquid is 1.5%, the mass ratio of sodium carboxymethyl cellulose and B liquid is 1:50, according to implementing 2 Preparation Method Viscose fibers containing Coralia pratense extract were prepared.
实施例9分散剂添加量单因素分析实验Example 9 Dispersant Addition Single Factor Analysis Experiment
采用实施例10-15所述的分散剂,分散剂种类为脂肪酸磺烷基酯,羧甲基纤维素钠和B液的质量比均为1:50,按照实施例2的制备方法制备含有草珊瑚提取物的粘胶纤维。 Using the dispersant described in Examples 10-15, the type of dispersant is fatty acid sulfoalkyl ester, the mass ratio of sodium carboxymethyl cellulose and liquid B is 1:50, and the preparation method of Example 2 is used to prepare the Viscose with coral extract.
实施例16羧甲基纤维素钠添加比例单因素分析实验Example 16 Carboxymethylcellulose sodium addition ratio single factor analysis experiment
采用实施例17-22所述的羧甲基纤维素钠和B液的配比,分散剂种类均为脂肪酸磺烷基酯,分散剂的添加量占A液的质量比均为1.5%,按照实施例2的制备方法制备含有草珊瑚提取物的粘胶纤维。 Adopt the proportioning of carboxymethylcellulose sodium described in embodiment 17-22 and B liquid, the type of dispersant is fatty acid sulfoalkyl ester, the mass ratio that the amount of dispersant accounts for A liquid is 1.5%, according to The preparation method of Example 2 prepared the viscose fiber containing the extract of Coralia praecox.
实施例23抗菌性能测试Embodiment 23 antibacterial performance test
根据GB-T20944.3-2008《纺织品抗菌性能的评价第3部分:振荡法》的规定,经过检测机构国家生态纺织品质量监督检验中心对实施例4-8、10-15、17-22中获得的粘胶纤维分别进行了抗菌能力的测试,结果见表1。 According to the provisions of GB-T20944.3-2008 "Evaluation of Antibacterial Properties of Textiles Part 3: Oscillating Method", after the National Ecological Textile Quality Supervision and Inspection Center of the testing agency obtained in Examples 4-8, 10-15, and 17-22 The antibacterial ability of the viscose fiber was tested respectively, and the results are shown in Table 1.
表1Table 1
由表1可见, It can be seen from Table 1 that
(1)分散剂种类单因素分析实验: (1) Single factor analysis experiment of dispersant type:
涉及实施例为4-8,结果显示,实施例6是优选的实施例; Relating to embodiment is 4-8, and the result shows that embodiment 6 is a preferred embodiment;
(2)分散剂添加量单因素分析实验: (2) Single factor analysis experiment of dispersant addition amount:
涉及实施例为10-15,结果显示,实施例12、13、14是优选实施例; Relating to embodiment 10-15, the result shows that embodiment 12, 13, 14 are preferred embodiments;
(3)羧甲基纤维素钠添加比例单因素分析实验: (3) Single factor analysis experiment of sodium carboxymethyl cellulose addition ratio:
涉及实施例17-22,结果显示,实施例19、20、21是优选实施例。 Regarding Examples 17-22, the results show that Examples 19, 20, and 21 are preferred examples.
实施例24粘胶纤维基本性能测试Embodiment 24 Viscose fiber basic performance test
对实施例4-8、10-15、17-22制得的粘胶纤维,按照GB/T14463-2008,进行技术性能测试,结果见表2 The viscose fiber that embodiment 4-8, 10-15, 17-22 makes, according to GB/T14463-2008, carries out technical performance test, and the results are shown in Table 2
表2 Table 2
由表2可见: It can be seen from Table 2:
(1)分散剂种类单因素分析实验: (1) Single factor analysis experiment of dispersant type:
涉及实施例为4-8,结果显示,实施例6是优选的实施例; Relating to embodiment is 4-8, and the result shows that embodiment 6 is a preferred embodiment;
(2)分散剂添加量单因素分析实验: (2) Single factor analysis experiment of dispersant addition amount:
涉及实施例为10-15,结果显示,实施例12、13是优选实施例; Relating to embodiment is 10-15, the result shows, embodiment 12, 13 is preferred embodiment;
(3)羧甲基纤维素钠添加比例单因素分析实验: (3) Single factor analysis experiment of sodium carboxymethyl cellulose addition ratio:
涉及实施例17-22,结果显示,实施例19、20是优选实施例。 Referring to Examples 17-22, the results show that Examples 19 and 20 are preferred examples.
通过对分散剂种类、分散剂添加量、羧甲基纤维素钠添加比例分别进行单因素分析实验,结合抗菌性能测试及粘胶纤维基本性能测试结果,综合得出,分散剂的最优种类为脂肪酸磺烷基酯,分散剂占A液的最优质量比为1.5-2.0%,羧甲基纤维素钠:B液的最优质量比为1:50-60。 Through the single factor analysis experiments on the type of dispersant, the amount of dispersant added, and the proportion of sodium carboxymethyl cellulose, combined with the results of the antibacterial performance test and the basic performance test of viscose fiber, it is concluded that the optimal type of dispersant is Fatty acid sulfoalkyl ester, the optimal mass ratio of dispersant to liquid A is 1.5-2.0%, and the optimal mass ratio of sodium carboxymethyl cellulose: liquid B is 1:50-60.
实施例25Example 25
一种含草珊瑚提取物的粘胶纤维的制备方法,包括以下步骤: A preparation method of viscose fiber containing a grass coral extract, comprising the following steps:
(1)抗菌剂溶液的制备:将草珊瑚提取物粉末加入到温度为25±1℃的水中,加入量为100g/1000ml水,充分搅拌至粉末完全溶解制成抗菌剂溶液,得A液。 (1) Preparation of antibacterial agent solution: Add the powdered coral coral extract to water at a temperature of 25±1°C in an amount of 100g/1000ml of water, stir well until the powder is completely dissolved to make an antibacterial agent solution, and obtain liquid A.
(2)加入分散剂:向上述A液中加入分散剂脂肪酸磺烷基酯,分散剂占A液的质量百分比为1.5%,搅拌,得B液。 (2) Adding a dispersant: Add a dispersant fatty acid sulfoalkyl ester to the above liquid A, the dispersant accounts for 1.5% by mass of the liquid A, stir to obtain liquid B.
(3)加入羧甲基纤维素钠 (3) Add carboxymethyl cellulose sodium
将羧甲基纤维素钠粉按质量比为1:50的比例,在50~60℃的温度范围内,边搅拌边加入上述B液中,得C液。 Add carboxymethyl cellulose sodium powder into the above liquid B while stirring at a temperature range of 50-60°C at a mass ratio of 1:50 to obtain liquid C.
(4)和纺丝原液共混 (4) Blending with spinning dope
将上述C液,按照纺丝原液15%的质量比,添加到纺丝原液中,搅拌分散后静置真空排泡,得D液。 The above liquid C was added to the spinning stock solution at a mass ratio of 15% of the spinning stock solution, stirred and dispersed, and then left to stand for vacuum defoaming to obtain liquid D.
(5)纺丝 (5) spinning
上述D液经计量泵计量后经烛形滤器和喷丝头进入10℃凝固浴;所述的凝固浴由20g/L硫酸,35g/L硫酸钠和10g/L硫酸锌组成,纺丝速度为15m/min。 Above-mentioned D liquid enters 10 ℃ of coagulation baths through candle filter and spinneret after metering pump metering; Described coagulation bath is made up of 20g/L sulfuric acid, 35g/L sodium sulfate and 10g/L zinc sulfate, and spinning speed is 15m/min.
(6)后处理 (6) Post-processing
经过脱硫、水洗、上油、烘干工序,制得本发明产品。 After desulfurization, water washing, oiling and drying processes, the product of the present invention is obtained.
实施例26Example 26
一种含草珊瑚提取物的粘胶纤维的制备方法,包括以下步骤: A preparation method of viscose fiber containing a grass coral extract, comprising the following steps:
(1)抗菌剂溶液的制备: (1) Preparation of antibacterial agent solution:
按照实施例25中抗菌剂溶液的制备步骤进行制备。 Prepare according to the preparation steps of the antibacterial agent solution in Example 25.
(2)加入分散剂:向上述A液中加入分散剂脂肪酸磺烷基酯,分散剂占A液的质量百分比为1.8%,搅拌,得B液。 (2) Adding a dispersant: add a dispersant fatty acid sulfoalkyl ester to the above liquid A, the dispersant accounts for 1.8% by mass of the liquid A, and stir to obtain a liquid B.
(3)加入羧甲基纤维素钠 (3) Add carboxymethyl cellulose sodium
将羧甲基纤维素钠粉按质量比为1:55的比例,在50~60℃的温度范围内,边搅拌边加入上述B液中,得C液。 Add carboxymethylcellulose sodium powder into the above liquid B while stirring at a temperature range of 50-60°C at a mass ratio of 1:55 to obtain liquid C.
(4)和纺丝原液共混 (4) Blending with spinning dope
将上述C液,按照纺丝原液16%的质量比,添加到纺丝原液中,搅拌分散后静置真空排泡,得D液。 The above liquid C was added to the spinning stock solution at a mass ratio of 16% of the spinning stock solution, stirred and dispersed, and then left to stand for vacuum defoaming to obtain D liquid.
(5)纺丝 (5) spinning
上述D液经计量泵计量后经烛形滤器和喷丝头进入13℃凝固浴;所述的凝固浴由22g/L硫酸,36g/L硫酸钠和13g/L硫酸锌组成,纺丝速度为18m/min。 Above-mentioned D liquid enters 13 ℃ of coagulation baths through candle filter and spinneret after metering pump metering; Described coagulation bath is made up of 22g/L sulfuric acid, 36g/L sodium sulfate and 13g/L zinc sulfate, and spinning speed is 18m/min.
(6)后处理 (6) Post-processing
经过脱硫、水洗、上油、烘干工序,制得本发明产品。 After desulfurization, water washing, oiling and drying processes, the product of the present invention is obtained.
实施例27Example 27
一种含草珊瑚提取物的粘胶纤维的制备方法,包括以下步骤: A preparation method of viscose fiber containing a grass coral extract, comprising the following steps:
(1)抗菌剂溶液的制备: (1) Preparation of antibacterial agent solution:
按照实施例25中抗菌剂溶液的制备步骤进行制备。 Prepare according to the preparation steps of the antibacterial agent solution in Example 25.
(2)加入分散剂:向上述A液中加入分散剂脂肪酸磺烷基酯,分散剂占A液的质量百分比为2%,搅拌,得B液。 (2) Adding a dispersant: Add a dispersant fatty acid sulfoalkyl ester to the above liquid A, the dispersant accounts for 2% by mass of the liquid A, stir to obtain liquid B.
(3)加入羧甲基纤维素钠 (3) Add carboxymethyl cellulose sodium
将羧甲基纤维素钠粉按质量比为1:60的比例,在50~60℃的温度范围内,边搅拌边加入上述B液中,得C液。 Add carboxymethyl cellulose sodium powder into the above liquid B while stirring at a temperature range of 50-60°C at a mass ratio of 1:60 to obtain liquid C.
(4)和纺丝原液共混 (4) Blending with spinning dope
将上述C液,按照纺丝原液17%的质量比,添加到纺丝原液中,搅拌分散后静置真空排泡,得D液。 The above liquid C was added to the spinning stock solution at a mass ratio of 17% of the spinning stock solution, stirred and dispersed, and then left to stand for vacuum defoaming to obtain liquid D.
(5)纺丝 (5) spinning
上述D液经计量泵计量后经烛形滤器和喷丝头进入14℃凝固浴;所述的凝固浴由25g/L硫酸,38g/L硫酸钠和15g/L硫酸锌组成,纺丝速度为40m/min。 Above-mentioned D liquid enters 14 ℃ of coagulation baths through candle filter and spinneret after metering pump metering; Described coagulation bath is made up of 25g/L sulfuric acid, 38g/L sodium sulfate and 15g/L zinc sulfate, and spinning speed is 40m/min.
(6)后处理 (6) Post-processing
经过脱硫、水洗、上油、烘干工序,制得本发明产品。 After desulfurization, water washing, oiling and drying processes, the product of the present invention is obtained.
实施例28抗菌性能测试结果Embodiment 28 antibacterial performance test result
根据GB-T20944.3-2008《纺织品抗菌性能的评价第3部分:振荡法》的规定,经过检测机构国家生态纺织品质量监督检验中心对实施例25、26、27中获得的粘胶纤维分别进行了抗菌能力的测试,结果见表3。 According to the provisions of GB-T20944.3-2008 "Evaluation of Antibacterial Performance of Textiles Part 3: Oscillating Method", the viscose fibers obtained in Examples 25, 26, and 27 were respectively tested by the testing agency National Ecological Textile Quality Supervision and Inspection Center. The antibacterial ability was tested, and the results are shown in Table 3.
表3 table 3
实施例29粘胶纤维基本性能测试结果Embodiment 29 viscose fiber basic performance test result
对实施例25、26、27制得的粘胶纤维,按照GB/T14463-2008,进行技术性能测试,结果见表4。 The viscose fibers prepared in Examples 25, 26, and 27 were tested for technical performance according to GB/T14463-2008, and the results are shown in Table 4.
表4 Table 4
最后应说明的是:以上所述仅为本发明的优选实施例而已,并不用于限制本发明,尽管参照前述实施例对本发明进行了详细说明,对于本领域的技术人员来说,其依然可以对前述各实施例所记载的技术方案进行修改,或者对其中部分技术特征进行等同替换。凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。 Finally, it should be noted that: the above is only a preferred embodiment of the present invention, and is not intended to limit the present invention. Although the present invention has been described in detail with reference to the foregoing embodiments, for those skilled in the art, it can still The technical solutions recorded in the foregoing embodiments are modified, or some of the technical features are equivalently replaced. Any modifications, equivalent replacements, improvements, etc. made within the spirit and principles of the present invention shall be included within the protection scope of the present invention.
Claims (8)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510176510.9A CN104790055B (en) | 2015-04-15 | 2015-04-15 | A kind of preparation method of viscose fiber containing grass coral extract |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510176510.9A CN104790055B (en) | 2015-04-15 | 2015-04-15 | A kind of preparation method of viscose fiber containing grass coral extract |
Publications (2)
Publication Number | Publication Date |
---|---|
CN104790055A CN104790055A (en) | 2015-07-22 |
CN104790055B true CN104790055B (en) | 2016-03-23 |
Family
ID=53555230
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201510176510.9A Active CN104790055B (en) | 2015-04-15 | 2015-04-15 | A kind of preparation method of viscose fiber containing grass coral extract |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN104790055B (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105316784A (en) * | 2015-12-02 | 2016-02-10 | 山传雷 | Composite microcapsule additive containing phase change material and sarcandra glabra extract and application of composite microcapsule additive |
CN106995943B (en) * | 2017-03-24 | 2018-08-07 | 青岛邦特生态纺织科技有限公司 | A kind of Chloranthus glaber efficient antibacterial antiviral cellulose fibre and preparation method thereof |
CN107641849A (en) * | 2017-09-15 | 2018-01-30 | 安徽宏祥丝绸织造有限公司 | A kind of preparation method of elastic force bubble satin antibacterial polyurethane fiber |
CN108166259A (en) * | 2018-01-10 | 2018-06-15 | 上海高聚生物科技有限公司 | A kind of non-woven cloth composite antibacterial agent and preparation method thereof |
CN109137181A (en) * | 2018-08-14 | 2019-01-04 | 何小莹 | A kind of Chloranthus glaber linen blend yarn |
CN110257940B (en) * | 2019-05-31 | 2022-05-24 | 山东银鹰化纤有限公司 | Cattail pollen viscose fiber and preparation method thereof |
CN114059186B (en) * | 2021-11-04 | 2023-12-29 | 青岛邦特生态纺织科技有限公司 | Ginger extract fiber and preparation method thereof |
CN114687031A (en) * | 2022-03-02 | 2022-07-01 | 上海英伦宝贝儿童用品有限公司 | Sarcandra glabra constant-temperature antibacterial yarn and fabric |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09119016A (en) * | 1995-10-26 | 1997-05-06 | Kohjin Co Ltd | Antimicrobial rayon fiber and its production |
CN101876090A (en) * | 2010-04-01 | 2010-11-03 | 张继红 | Viscose fiber with anti-bacterial function and preparation method thereof |
CN102926013A (en) * | 2012-11-14 | 2013-02-13 | 单修铎 | Viscose containing natural antimicrobials and preparation method thereof |
CN103225123A (en) * | 2013-04-22 | 2013-07-31 | 青岛私衣橱柜纤维科技有限公司 | Viscose fiber with plant source anti-bacterial function and aromatic smell, and preparation method thereof |
CN103556250A (en) * | 2013-10-24 | 2014-02-05 | 恒天海龙股份有限公司 | Antibacterial viscose containing artemisia argyi oil component and production method of antibacterial viscose |
-
2015
- 2015-04-15 CN CN201510176510.9A patent/CN104790055B/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09119016A (en) * | 1995-10-26 | 1997-05-06 | Kohjin Co Ltd | Antimicrobial rayon fiber and its production |
CN101876090A (en) * | 2010-04-01 | 2010-11-03 | 张继红 | Viscose fiber with anti-bacterial function and preparation method thereof |
CN102926013A (en) * | 2012-11-14 | 2013-02-13 | 单修铎 | Viscose containing natural antimicrobials and preparation method thereof |
CN103225123A (en) * | 2013-04-22 | 2013-07-31 | 青岛私衣橱柜纤维科技有限公司 | Viscose fiber with plant source anti-bacterial function and aromatic smell, and preparation method thereof |
CN103556250A (en) * | 2013-10-24 | 2014-02-05 | 恒天海龙股份有限公司 | Antibacterial viscose containing artemisia argyi oil component and production method of antibacterial viscose |
Non-Patent Citations (1)
Title |
---|
草珊瑚粘胶纤维的制备及其性能的研究;陈翠翠;《青岛大学硕士学位论文》;20120715;第12页第1-2行,倒数第2行,第31页第1段,第34页第4.3节和第35页第4.5节 * |
Also Published As
Publication number | Publication date |
---|---|
CN104790055A (en) | 2015-07-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN106222777B (en) | A kind of preparation method of the mosquito repellent viscose rayon containing wormwood extract | |
CN104790055B (en) | A kind of preparation method of viscose fiber containing grass coral extract | |
CN104805520B (en) | A kind of preparation method of viscose fiber containing apocynum extract | |
CN103225123B (en) | Viscose fiber with plant source anti-bacterial function and aromatic smell, and preparation method thereof | |
CN102926013A (en) | Viscose containing natural antimicrobials and preparation method thereof | |
CN106048763B (en) | A kind of motherwort cellulose fibre and preparation method thereof | |
CN111534875B (en) | Efficient antibacterial antiviral isatis root viscose fiber and preparation method thereof | |
CN104963086A (en) | Alginate fiber anti-bacteria facial mask base cloth | |
CN110904522A (en) | Fullerene skin-friendly composite fiber and preparation method thereof | |
CN101240468A (en) | A kind of polyacrylonitrile-chitin composite fiber and its manufacturing method | |
CN103993377B (en) | A kind of antibiotic skin-care agent compositions and the viscose rayon prepared with it and preparation method | |
CN104372432A (en) | Preparation method of silver-bearing antibacterial polypropylene fiber | |
CN109056093A (en) | A kind of rosemary cellulose fibre and preparation method thereof | |
CN115029925A (en) | A kind of botanical traditional Chinese medicine composition and preparation method of mosquito repellent, antibacterial, mildewproof cotton fiber | |
CN103966690B (en) | The preparation method of silver oxide antibacterial viscose fiber and reaction in-situ thereof | |
CN106192045B (en) | A kind of Radix Isatidis cellulose fibre and preparation method thereof | |
CN103741452B (en) | A kind of shirt dressing liquid and preparation method thereof | |
CN108085781A (en) | A kind of preparation method of microballoon antibacterial colorant alginate fibre | |
CN104562273A (en) | Method for processing fishing net thread by nylon | |
CN104674375B (en) | A kind of preparation method of wig composite fibre | |
CN105369389A (en) | Collagen fiber and its production process | |
CN112342634A (en) | Preparation method of antibacterial nano cellulose fiber | |
CN112064131A (en) | Viscose containing dandelion and preparation method thereof | |
CN115074850A (en) | Antibacterial high-wet-modulus bamboo cellulose fiber and preparation method thereof | |
CN105113033A (en) | Preparation method of anti-bacterial and mite-proof sulfur-containing viscose fiber |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
EXSB | Decision made by sipo to initiate substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C41 | Transfer of patent application or patent right or utility model | ||
CB03 | Change of inventor or designer information |
Inventor after: Liu Yixin Inventor after: Li Minghua Inventor after: Jiang Mingliang Inventor before: Liu Yixin Inventor before: Jiang Mingliang |
|
COR | Change of bibliographic data | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20160222 Address after: 266071 Ningxia Road, Shandong, China, No. 308, No. Applicant after: QINGDAO University Applicant after: QINGDAO BAICAO FIBER TECHNOLOGY Co.,Ltd. Address before: 266071 Ningxia Road, Shandong,, No. 308, Qiingdao University Applicant before: Liu Yixin |
|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CP01 | Change in the name or title of a patent holder | ||
CP01 | Change in the name or title of a patent holder |
Address after: 266071 Ningxia Road, Shandong, China, No. 308, No. Patentee after: QINGDAO University Patentee after: BESTEE MATERIAL (TSINGTAO) Co.,Ltd. Address before: 266071 Ningxia Road, Shandong, China, No. 308, No. Patentee before: Qingdao University Patentee before: QINGDAO BAICAO FIBER TECHNOLOGY Co.,Ltd. |
|
CP03 | Change of name, title or address | ||
CP03 | Change of name, title or address |
Address after: 266071 No. 308, Ningxia Road, Qingdao, Shandong Patentee after: QINGDAO University Country or region after: China Patentee after: Baicao Future Health Technology (Qingdao) Co.,Ltd. Address before: 266071 No. 308, Ningxia Road, Qingdao, Shandong Patentee before: QINGDAO University Country or region before: China Patentee before: BESTEE MATERIAL (TSINGTAO) Co.,Ltd. |