天然染料对羊毛织物的微波辅助环保染色方法:第二部分。使用不同媒染剂的效果

M. El-Apasery, A. Hussein, M. Saleh, Abubaker A Eladasy, Nahed Nour El-Din
{"title":"天然染料对羊毛织物的微波辅助环保染色方法:第二部分。使用不同媒染剂的效果","authors":"M. El-Apasery, A. Hussein, M. Saleh, Abubaker A Eladasy, Nahed Nour El-Din","doi":"10.21608/EJCHEM.2021.72139.3589","DOIUrl":null,"url":null,"abstract":"Our current study aims to study the effect of different metallic mordantson the new natural dyes that we were able to extract in a previous study. The extent to which the intensity of color is affected by the presence of metallic mordantshave been studied and also the effect of the concentration of each mordant on the natural dyes was investigated, and then the changes that took place on the color axes were screened, and then the fastness of the new dyes were studied after applying them to the woolen fabric. Introduction Mordants are mineral salts added to the dyeing process in order to provide chemical bonds between the natural dye and the fabric. They improve the color fastness of the fabrics to be dyed due to easily bonding with natural dye [1-4]. There are some transitional elements that were used in the past as a mordant, such as Cu and Cr, but they are not currently recommended due to their environmental damage. Therefore, these harmful elements were replaced by other environmentally friendly elements such as aluminum, iron which used as a mordants to reduce potential harm to human health [5]. Alum usually refers to a hydrated double sulfate of potassium hydrogen sulfate (KAl (SO4)2.12H2O), which confers evenness and brightness on dyed fabrics; iron saddens or dulls the color. Tin is particularly used to achieve brighter colors; however, it might damage wool by making it brittle and rough to the touch [6]. The mordant can be applied before, after or simultaneously with dyeing, forming methods known as pre-mordanting, postmordanting and simultaneous mordanting [7, 8]. Another agent used to improve the color fastness of natural dyes on textiles is tannic acid [9-11]. The use of tannin compounds dates back to the 18 century when the quality and utility of animal skins were enhanced through the tannin process [12]. Regarding the dyeing of cotton or wool fabrics, tannic acid forms a color lake with dye inside the fiber which fixes dye to fibers more strongly [6]. It improves the color stability of the tissues to be dyed due to the ease of its association with the natural dye. Experimental  Metallic mordants. The wool fabrics dyed with D1, D2 and D3 dyes at the optimum values obtained as described before in our previouspaper [13]were mordanted with different mordant by simultaneous mordanting method. Ferrous sulphate, stannous chloride, potassium alumm. sulphate and copper sulphate were used as a metallic mordants.  Substrates Scoured and bleachedwool fabric waspurchased from Misr for Spinning and Weaving Company, Mahalla El-Kobra, Egypt.  Microwave assisted extraction The process ofextraction was carried out by using microwave. A Samsung oven model MS404MADXXBB.  Microwave dyeingmethod Egyptian Journal of Chemistry http://ejchem.journals.ekb.eg/ 353 Morsy Elapasery et.al. _____________________________________________________________________________________________________________ ________________________________________________ Egypt. J. Chem. 64, No. 7 (2021) 3762 The extracted dye were companied with metallic mordant in different concentration and then applied to wool fabrics with M: L ratio 1:100and the dyeing time was 1 hour.  Color measurements Reflectance Spectrophotometer is the device used to measure the intensity of color on dyed wool fabrics andlight reflection technology has been applied for that. The dye yield was determined on the dyed fabric using a spectrophotometer. Kubelka-Munk's Equation (1).Equation was applied to find out the intensity of the color of dye, which is symbolized by the symbol K/S[20]. K/S = [(1R) 2 / 2R] [(1Ro) 2 / 2Ro] (1) Where R is the reflectance of dyed samples, K is the absorption coefficient, S is the scattering coefficient, and Ro = decimal fraction of the reflectance of the undyed fabric.  Fastness properties 1Color fastness to washing The color stability to washing was determined by method of ISO 105-C02:1989 [21]. Aspecimen of the dyed fabric was placed between two bleached slices, one of them is cotton fabric and the other of the wool fabric, and attached with them byhand stitching, and then it was soaked in an aqueous solution consisting of 5 g/L of nonionic detergents at a liquor ratio of 1:50 for 30 minutes at of 60 °C and then sample was rinsed thoroughly with manual squeeze, and then sample was allowed to dry. Gray scale was applied to assess the color fastness to wash. 2Color fastness to perspiration Using L-histidine monohydro-chloride monohydrate (0.5 g), sodium chloride (5 g), and sodium dihydrogen orthophosphate dihydrate (2.2 g) in one liter of distilled water, a solution of artificial sweat was obtained. For have acidic sweat pH was adjusted to 5.5 by 0.1 N of NaOH and by the same way an alkaline sweat was obtained by adjusting pH of solution at 8.0.The fastness test was performed according to the following procedure: Between two different parts of uncolored patterns a sample of dyed fabric (5×4 cm) was sutured. The samples were soaked in both solutions undergoing agitation and pressing for 15-30 min to have perfect wetting. Sample undergo a load of 4-5 kg while the sample was placed between two plates of plastic or glass. Then these plates were placed at a temperature of 37 °C vertically for four hours, and then a gray scale change technique was used to assess the color fastness to perspiration 3Color fastness to light The method of measuring the stability of color fastness to light is ISO 105-B02:1988 test technique where the dyed sample placed for 35 hours to a carbon arc lamp and then using the blue color scale to investigate color change of the tested samples. 4Color fastness to rubbing By applying the technique of ISO 105-X12:1987 test the color fastness to crocking was determined. When dyed fabric undergoes rubbing, it is can be estimate if dye move from dyed fabric to another one or not. The wet and dry rubbing had been estimates. Results and discussion Optimization of mordant concentrations Different concentrations from metallic mordants were applied to dyeing process of wool by D1, D2 and D3 (from 0.02 gm/L to 0.1 gm/L) and then K/S was tested. Data of table 1 and Fig.1 show that the color strength increase by mordant concentration increasing and by using ferrous sulphate as a mordant color shift slightly toward darkness where (L) values decreased and from negative values of (a) and low positive values of (b) color shift from yellow zone to green zone. Stannous chloride gives new dye where (L) values refer that color move to darkness zone and high positive values of (b) low positive values of (a) indicate that dye go to yellow color. In the same behavior potassium alumm. Sulphate has low positive values of (a) and high positive value of (b) then dye found in yellow zone but it becomes darker and that was clear from low positive values of (L). Copper sulphate as a mordant with D1 produced new dye darker than original dye and dye which produced from ferrous sulphate and D1 that was clear from (L) values and negative values of (a) and low positive values of (b) show that dye found in green color zone. Fig. 2 refers that K/S values increased by increasing concentration of metallic mordants. Values of (L), (a) and (b) in table 8 indicate that mixing of ferrous sulphate with D2 color shift slightly toward darkness and color found green zone. Stannous chloride with D2 gives a dye present in darkness zone and go to yellow color due to (L), (a) and (b) values. Combination of Potassium alumm. Sulphate and D2 gives dye has low positive values of (a) and high positive value of (b) then dye found in yellow zone but it becomes darker and that was clear from low positive values of (L). The same behavior of the Copper sulphate as a mordant with D1 is seen when it combined with the D2where new dye is darker than original dye and dye found in green color zone. That is clearly from (L), (a) and (b) values. Fig.3 shows that increasing concentration of metallic mordants when they correlate with D3 leads to increasing in color intensity. MICROWAVE-ASSISTED DYEING OF WOOL FABRICS WITH NATURAL ...... __________________________________________________________________________________________________________________ ________________________________________________ Egypt. J. Chem. 64, No. 7 (2021) 3763 Information of table 9. Show that the selected metallic mordants have the same behavior with D3 when then mixed with it where dye which produced form mixing D3 with ferrous sulphate is dark and found in green zone. Mixture of D3 and stannous chloride produced dye found in dark area and yellow zone. Table 1. Effect of metallic mordant on D1. mordant Mordant conc. K / S L a b c h Without mordant 12.28 64.02 5.04 25.22 25.72 78.70 Ferric sulphate 0.02 9.83 51.52 0.54 10.12 10.13 93.03 0.04 12.35 44.03 0.89 9.76 9.80 95.22 0.06 12.75 45.32 1.24 19.17 9.26 97.69 0.08 13.34 43.33 0.77 10.06 10.09 94.40 0.10 17.85 44.43 1.20 9.02 9.10 97.59 Stannous chloride 0.02 14.85 56.69 2.28 29.84 29.93 85.63 0.04 15.19 52.08 1.71 29.92 29.97 86.73 0.06 16.38 51.40 1.20 29.21 29.23 87.65 0.08 17.98 52.07 0.59 28.14 28.15 88.81 0.10 18.94 52.11 0.49 27.27 27.28 91.03 Pothach. Aluom 0.02 18.31 72.34 6.68 45.37 45.45 86.62 0.04 19.03 71.77 5.25 55.26 55.50 84.57 0.06 19.6 71.29 6.02 58.80 59.10 84.16 0.08 22.10 71.84 6.80 63.86 64.22 83.92 0.10 23.47 72.94 6.27 62.42 62.73 84.27 Copper sulphate 0.02 9.77 69.21 0.04 32.15 32.15 90.07 0.04 10.33 70.01 0.19 33.50 33.50 89.67 0.06 10.65 70.23 0.21 35.46 35.46 89.66 0.08 10.78 71.65 0.02 35.48 35.48 90.04 0.10 13.42 72.06 0.20 33.71 33.71 89.66 Fig. 1. Effect of metallic mordant concentration on D1 Morsy Elapasery et.al. _____________________________________________________________________________________________________________ ________________________________________________ Egypt. J. Chem. 64, No. 7 (2021) 3764 Table 2. Effect of metallic mordant on D2. mordant Mordant conc. K / S L a b c h Without mordant 8.86 65.96 4.59 24.49 24.92 79.3","PeriodicalId":22429,"journal":{"name":"The Egyptian Journal of Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2021-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Microwave-assisted dyeing of wool fabrics with natural dyes as eco- friendly dyeing method: part II. The effect of using different mordants\",\"authors\":\"M. El-Apasery, A. Hussein, M. Saleh, Abubaker A Eladasy, Nahed Nour El-Din\",\"doi\":\"10.21608/EJCHEM.2021.72139.3589\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Our current study aims to study the effect of different metallic mordantson the new natural dyes that we were able to extract in a previous study. The extent to which the intensity of color is affected by the presence of metallic mordantshave been studied and also the effect of the concentration of each mordant on the natural dyes was investigated, and then the changes that took place on the color axes were screened, and then the fastness of the new dyes were studied after applying them to the woolen fabric. Introduction Mordants are mineral salts added to the dyeing process in order to provide chemical bonds between the natural dye and the fabric. They improve the color fastness of the fabrics to be dyed due to easily bonding with natural dye [1-4]. There are some transitional elements that were used in the past as a mordant, such as Cu and Cr, but they are not currently recommended due to their environmental damage. Therefore, these harmful elements were replaced by other environmentally friendly elements such as aluminum, iron which used as a mordants to reduce potential harm to human health [5]. Alum usually refers to a hydrated double sulfate of potassium hydrogen sulfate (KAl (SO4)2.12H2O), which confers evenness and brightness on dyed fabrics; iron saddens or dulls the color. Tin is particularly used to achieve brighter colors; however, it might damage wool by making it brittle and rough to the touch [6]. The mordant can be applied before, after or simultaneously with dyeing, forming methods known as pre-mordanting, postmordanting and simultaneous mordanting [7, 8]. Another agent used to improve the color fastness of natural dyes on textiles is tannic acid [9-11]. The use of tannin compounds dates back to the 18 century when the quality and utility of animal skins were enhanced through the tannin process [12]. Regarding the dyeing of cotton or wool fabrics, tannic acid forms a color lake with dye inside the fiber which fixes dye to fibers more strongly [6]. It improves the color stability of the tissues to be dyed due to the ease of its association with the natural dye. Experimental  Metallic mordants. The wool fabrics dyed with D1, D2 and D3 dyes at the optimum values obtained as described before in our previouspaper [13]were mordanted with different mordant by simultaneous mordanting method. Ferrous sulphate, stannous chloride, potassium alumm. sulphate and copper sulphate were used as a metallic mordants.  Substrates Scoured and bleachedwool fabric waspurchased from Misr for Spinning and Weaving Company, Mahalla El-Kobra, Egypt.  Microwave assisted extraction The process ofextraction was carried out by using microwave. A Samsung oven model MS404MADXXBB.  Microwave dyeingmethod Egyptian Journal of Chemistry http://ejchem.journals.ekb.eg/ 353 Morsy Elapasery et.al. _____________________________________________________________________________________________________________ ________________________________________________ Egypt. J. Chem. 64, No. 7 (2021) 3762 The extracted dye were companied with metallic mordant in different concentration and then applied to wool fabrics with M: L ratio 1:100and the dyeing time was 1 hour.  Color measurements Reflectance Spectrophotometer is the device used to measure the intensity of color on dyed wool fabrics andlight reflection technology has been applied for that. The dye yield was determined on the dyed fabric using a spectrophotometer. Kubelka-Munk's Equation (1).Equation was applied to find out the intensity of the color of dye, which is symbolized by the symbol K/S[20]. K/S = [(1R) 2 / 2R] [(1Ro) 2 / 2Ro] (1) Where R is the reflectance of dyed samples, K is the absorption coefficient, S is the scattering coefficient, and Ro = decimal fraction of the reflectance of the undyed fabric.  Fastness properties 1Color fastness to washing The color stability to washing was determined by method of ISO 105-C02:1989 [21]. Aspecimen of the dyed fabric was placed between two bleached slices, one of them is cotton fabric and the other of the wool fabric, and attached with them byhand stitching, and then it was soaked in an aqueous solution consisting of 5 g/L of nonionic detergents at a liquor ratio of 1:50 for 30 minutes at of 60 °C and then sample was rinsed thoroughly with manual squeeze, and then sample was allowed to dry. Gray scale was applied to assess the color fastness to wash. 2Color fastness to perspiration Using L-histidine monohydro-chloride monohydrate (0.5 g), sodium chloride (5 g), and sodium dihydrogen orthophosphate dihydrate (2.2 g) in one liter of distilled water, a solution of artificial sweat was obtained. For have acidic sweat pH was adjusted to 5.5 by 0.1 N of NaOH and by the same way an alkaline sweat was obtained by adjusting pH of solution at 8.0.The fastness test was performed according to the following procedure: Between two different parts of uncolored patterns a sample of dyed fabric (5×4 cm) was sutured. The samples were soaked in both solutions undergoing agitation and pressing for 15-30 min to have perfect wetting. Sample undergo a load of 4-5 kg while the sample was placed between two plates of plastic or glass. Then these plates were placed at a temperature of 37 °C vertically for four hours, and then a gray scale change technique was used to assess the color fastness to perspiration 3Color fastness to light The method of measuring the stability of color fastness to light is ISO 105-B02:1988 test technique where the dyed sample placed for 35 hours to a carbon arc lamp and then using the blue color scale to investigate color change of the tested samples. 4Color fastness to rubbing By applying the technique of ISO 105-X12:1987 test the color fastness to crocking was determined. When dyed fabric undergoes rubbing, it is can be estimate if dye move from dyed fabric to another one or not. The wet and dry rubbing had been estimates. Results and discussion Optimization of mordant concentrations Different concentrations from metallic mordants were applied to dyeing process of wool by D1, D2 and D3 (from 0.02 gm/L to 0.1 gm/L) and then K/S was tested. Data of table 1 and Fig.1 show that the color strength increase by mordant concentration increasing and by using ferrous sulphate as a mordant color shift slightly toward darkness where (L) values decreased and from negative values of (a) and low positive values of (b) color shift from yellow zone to green zone. Stannous chloride gives new dye where (L) values refer that color move to darkness zone and high positive values of (b) low positive values of (a) indicate that dye go to yellow color. In the same behavior potassium alumm. Sulphate has low positive values of (a) and high positive value of (b) then dye found in yellow zone but it becomes darker and that was clear from low positive values of (L). Copper sulphate as a mordant with D1 produced new dye darker than original dye and dye which produced from ferrous sulphate and D1 that was clear from (L) values and negative values of (a) and low positive values of (b) show that dye found in green color zone. Fig. 2 refers that K/S values increased by increasing concentration of metallic mordants. Values of (L), (a) and (b) in table 8 indicate that mixing of ferrous sulphate with D2 color shift slightly toward darkness and color found green zone. Stannous chloride with D2 gives a dye present in darkness zone and go to yellow color due to (L), (a) and (b) values. Combination of Potassium alumm. Sulphate and D2 gives dye has low positive values of (a) and high positive value of (b) then dye found in yellow zone but it becomes darker and that was clear from low positive values of (L). The same behavior of the Copper sulphate as a mordant with D1 is seen when it combined with the D2where new dye is darker than original dye and dye found in green color zone. That is clearly from (L), (a) and (b) values. Fig.3 shows that increasing concentration of metallic mordants when they correlate with D3 leads to increasing in color intensity. MICROWAVE-ASSISTED DYEING OF WOOL FABRICS WITH NATURAL ...... __________________________________________________________________________________________________________________ ________________________________________________ Egypt. J. Chem. 64, No. 7 (2021) 3763 Information of table 9. Show that the selected metallic mordants have the same behavior with D3 when then mixed with it where dye which produced form mixing D3 with ferrous sulphate is dark and found in green zone. Mixture of D3 and stannous chloride produced dye found in dark area and yellow zone. Table 1. Effect of metallic mordant on D1. mordant Mordant conc. K / S L a b c h Without mordant 12.28 64.02 5.04 25.22 25.72 78.70 Ferric sulphate 0.02 9.83 51.52 0.54 10.12 10.13 93.03 0.04 12.35 44.03 0.89 9.76 9.80 95.22 0.06 12.75 45.32 1.24 19.17 9.26 97.69 0.08 13.34 43.33 0.77 10.06 10.09 94.40 0.10 17.85 44.43 1.20 9.02 9.10 97.59 Stannous chloride 0.02 14.85 56.69 2.28 29.84 29.93 85.63 0.04 15.19 52.08 1.71 29.92 29.97 86.73 0.06 16.38 51.40 1.20 29.21 29.23 87.65 0.08 17.98 52.07 0.59 28.14 28.15 88.81 0.10 18.94 52.11 0.49 27.27 27.28 91.03 Pothach. Aluom 0.02 18.31 72.34 6.68 45.37 45.45 86.62 0.04 19.03 71.77 5.25 55.26 55.50 84.57 0.06 19.6 71.29 6.02 58.80 59.10 84.16 0.08 22.10 71.84 6.80 63.86 64.22 83.92 0.10 23.47 72.94 6.27 62.42 62.73 84.27 Copper sulphate 0.02 9.77 69.21 0.04 32.15 32.15 90.07 0.04 10.33 70.01 0.19 33.50 33.50 89.67 0.06 10.65 70.23 0.21 35.46 35.46 89.66 0.08 10.78 71.65 0.02 35.48 35.48 90.04 0.10 13.42 72.06 0.20 33.71 33.71 89.66 Fig. 1. Effect of metallic mordant concentration on D1 Morsy Elapasery et.al. _____________________________________________________________________________________________________________ ________________________________________________ Egypt. J. Chem. 64, No. 7 (2021) 3764 Table 2. Effect of metallic mordant on D2. mordant Mordant conc. K / S L a b c h Without mordant 8.86 65.96 4.59 24.49 24.92 79.3\",\"PeriodicalId\":22429,\"journal\":{\"name\":\"The Egyptian Journal of Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-04-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Egyptian Journal of Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21608/EJCHEM.2021.72139.3589\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Egyptian Journal of Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/EJCHEM.2021.72139.3589","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

摘要

本研究的目的是研究不同金属盐对我们在前人研究中提取的新型天然染料的影响。研究了金属媒染剂的存在对颜色强度的影响程度,以及每种媒染剂的浓度对天然染料的影响,筛选了天然染料在色轴上的变化,并研究了新染料在毛织品上的牢度。媒染剂是在染色过程中添加的矿物盐,目的是在天然染料和织物之间提供化学键。由于易于与天然染料结合,它们提高了待染色织物的色牢度[1-4]。有一些过渡元素在过去被用作媒染剂,如Cu和Cr,但由于它们对环境的破坏,目前不推荐使用。因此,这些有害元素被铝、铁等其他环保元素取代,作为媒染剂使用,以减少对人体健康的潜在危害[5]。明矾通常是指硫酸氢钾(KAl (SO4)2.12H2O)的水合双硫酸盐,它赋予染色织物均匀度和亮度;铁使颜色暗淡。锡特别用于实现更明亮的颜色;然而,它可能会使羊毛变脆,摸起来粗糙,从而损害羊毛[6]。媒染剂可在染色前、染色后或与染色同时使用,形成方法称为预媒染法、后媒染法和同时媒染法[7,8]。另一种用于提高纺织品天然染料色牢度的剂是单宁酸[9-11]。单宁化合物的使用可以追溯到18世纪,当时通过单宁工艺提高了动物皮的质量和效用[12]。对于棉毛织物的染色,单宁酸与纤维内的染料形成色湖,使染料对纤维的固定性更强[6]。由于易于与天然染料结合,它改善了待染色组织的颜色稳定性。实验性金属媒染剂。用D1、D2和D3染料染色的羊毛织物,在我们之前的论文[13]中得到的最佳染色值,用不同的媒染剂进行同步媒染法。硫酸亚铁,氯化亚锡,铝钾。硫酸盐和硫酸铜被用作金属媒染剂。◆基材经洗涤和漂白的羊毛织物购自Misr纺纱和织造公司,Mahalla El-Kobra,埃及。微波辅助提取采用微波辅助提取。三星烤箱型号MS404MADXXBB。微波染色法埃及化学杂志http://ejchem.journals.ekb.eg/ 353 Morsy Elapasery等。_____________________________________________________________________________________________________________ ________________________________________________ 埃及。将提取的染料与不同浓度的金属媒染剂配伍,以M: L比1:100应用于羊毛织物,染色时间为1小时。反射分光光度计是用于测量染色羊毛织物颜色强度的设备,光反射技术已被应用于该设备。用分光光度计测定染色织物上的染料得率。Kubelka-Munk’S Equation(1):用该方程求出染料颜色的强度,用K/S符号表示[20]。K/S = [(1R) 2 / 2R] [(1Ro) 2 / 2Ro](1)式中,R为染色样品的反射率,K为吸收系数,S为散射系数,Ro为未染色织物反射率的小数部分。牢度性能1耐洗色牢度耐洗色稳定性按ISO 105-C02:1989[21]的方法测定。将染色织物的试样置于棉织物和羊毛织物的两块漂白片之间,用手缝线贴在一起,然后在含5 g/L非离子洗涤剂的水溶液中,以1:50的液比浸泡30分钟,温度为60℃,然后用手挤压彻底冲洗,晾干。采用灰度等级评定耐洗色牢度。用l -组氨酸一氢氯化钠(0.5 g)、氯化钠(5 g)、正磷酸二氢钠二水(2.2 g)加入1升蒸馏水,制得人工汗液。用0.1 N NaOH将酸性汗液pH调节到5.5,用同样的方法将溶液pH调节到8.0得到碱性汗液。牢度测试按以下步骤进行:在未着色图案的两个不同部分之间缝合染色织物样品(5×4 cm)。 样品在两种溶液中浸泡,搅拌和压制15-30分钟,以达到完全润湿。当样品放置在两个塑料或玻璃板之间时,样品承受4-5公斤的负荷。然后在37℃的温度下垂直放置4小时,然后用灰度变化技术评估耐汗色牢度。耐光色牢度稳定性的测量方法是ISO 105- b2:1988测试技术,将染色后的样品在碳弧灯下放置35小时,然后用蓝色色标来研究被测样品的颜色变化。耐摩擦色牢度采用ISO 105-X12:1987试验技术,测定了耐摩擦色牢度。当染色织物发生摩擦时,可以判断染料是否从染色织物转移到另一种织物。湿的和干的摩擦已经被估计过了。将不同浓度的金属媒染剂D1、D2和D3(从0.02 gm/L到0.1 gm/L)应用于羊毛染色过程,并测定K/S。从表1和图1的数据可以看出,颜色强度随着媒染剂浓度的增加而增加,使用硫酸亚铁作为媒染剂,颜色稍微向暗方向移动,其中(L)值减小,颜色由(a)的负值和(b)的低正值从黄色区域向绿色区域移动。氯化亚锡得到新的染料,其中(L)值表示颜色移至暗区,(b)值高,(a)值低,表示染料变为黄色。在相同的行为钾铝。硫酸低积极的价值观(a)和高正值(b)然后染料中黄色区域变得黑暗,但显然从低(L)的积极价值。硫酸铜作为媒染剂D1产生新的染料比原染料和染料生产从硫酸亚铁和D1清楚(L)值和负的(a)和(b)表明,正值低的染料在绿色区域。从图2可以看出,K/S值随着金属媒染剂浓度的增加而增加。表8中(L)、(a)、(b)的值表明,硫酸亚铁与D2混合后颜色略微偏暗,颜色出现绿区。含D2的氯化亚锡使染料呈现在暗区,并由于(L)、(a)和(b)值而变为黄色。钾铝的组合。硫酸盐和D2使染料具有(a)的低正值和(b)的高正值,然后在黄色区域中发现染料,但它变得更暗,这从(L)的低正值中可以清楚地看到。当与D2结合时,可以看到硫酸铜作为媒染剂与D1的相同行为,其中新染料比原始染料和绿色区域中的染料更深。这显然是由(L) (a)和(b)的值得出的。从图3可以看出,当金属媒染剂与D3相关时,其浓度的增加会导致颜色强度的增加。微波辅助染色羊毛织物与天然......__________________________________________________________________________________________________________________ ________________________________________________ 埃及。化学学报,64,No. 7 (2021) 3763表明所选择的金属媒染剂与D3混合后具有相同的行为,其中D3与硫酸亚铁混合后产生的染料颜色较深,位于绿色区域。D3和氯化亚锡的混合物产生的染料在暗区和黄区发现。表1。金属媒染剂对D1的影响。媒质;媒质;K / S L a b c h没有媒介12.28 64.02 5.04 25.22 25.72 78.70铁硫酸盐0.02 9.83 51.52 0.54 10.12 10.13 93.03 0.04 12.35 44.03 0.89 9.76 9.80 95.22 0.06 12.75 45.32 1.24 19.17 9.26 97.69 0.08 13.34 43.33 0.77 10.06 10.09 94.40 0.10 17.85 44.43 1.20 9.02 9.10 97.59氯化亚锡0.02 14.85 56.69 2.28 29.84 29.93 85.63 0.04 15.19 52.08 1.71 29.92 29.97 86.73 0.06 16.38 51.40 1.20 29.21 29.23 87.65 0.08 17.98 52.07 0.59 28.14 28.15 88.81 0.10 18.94 52.11 0.49 27.27 27.28 91.03Pothach。氧化铝0.02 18.31 72.34 6.68 45.37 45.45 86.62 0.04 19.03 71.77 5.25 55.26 55.50 84.57 0.06 19.6 71.29 6.02 58.80 59.10 84.16 0.08 22.10 71.84 6.80 63.86 64.22 83.92 0.10 23.47 72.94 6.27 62.42 62.73 84.27硫酸铜0.02 9.77 69.21 0.04 32.15 32.15 90.07 0.04 10.33 70.01 0.19 33.50 33.50 89.67 0.06 10.65 70.23 0.21 35.46 35.46 89.66 0.08 10.78 71.65 0.02 35.48 35.48 90.04 0.10 13.42 72.06 0.20 33.71 89.66图1金属媒染剂浓度对D1 Morsy elapery等的影响。_____________________________________________________________________________________________________________ ________________________________________________ 埃及。化学学报,64,No. 7 (2021) 3764金属媒染剂对D2的影响。媒质;媒质; K / S L a b c h无媒染剂8.86 65.96 4.59 24.49 24.92 79.3
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Microwave-assisted dyeing of wool fabrics with natural dyes as eco- friendly dyeing method: part II. The effect of using different mordants
Our current study aims to study the effect of different metallic mordantson the new natural dyes that we were able to extract in a previous study. The extent to which the intensity of color is affected by the presence of metallic mordantshave been studied and also the effect of the concentration of each mordant on the natural dyes was investigated, and then the changes that took place on the color axes were screened, and then the fastness of the new dyes were studied after applying them to the woolen fabric. Introduction Mordants are mineral salts added to the dyeing process in order to provide chemical bonds between the natural dye and the fabric. They improve the color fastness of the fabrics to be dyed due to easily bonding with natural dye [1-4]. There are some transitional elements that were used in the past as a mordant, such as Cu and Cr, but they are not currently recommended due to their environmental damage. Therefore, these harmful elements were replaced by other environmentally friendly elements such as aluminum, iron which used as a mordants to reduce potential harm to human health [5]. Alum usually refers to a hydrated double sulfate of potassium hydrogen sulfate (KAl (SO4)2.12H2O), which confers evenness and brightness on dyed fabrics; iron saddens or dulls the color. Tin is particularly used to achieve brighter colors; however, it might damage wool by making it brittle and rough to the touch [6]. The mordant can be applied before, after or simultaneously with dyeing, forming methods known as pre-mordanting, postmordanting and simultaneous mordanting [7, 8]. Another agent used to improve the color fastness of natural dyes on textiles is tannic acid [9-11]. The use of tannin compounds dates back to the 18 century when the quality and utility of animal skins were enhanced through the tannin process [12]. Regarding the dyeing of cotton or wool fabrics, tannic acid forms a color lake with dye inside the fiber which fixes dye to fibers more strongly [6]. It improves the color stability of the tissues to be dyed due to the ease of its association with the natural dye. Experimental  Metallic mordants. The wool fabrics dyed with D1, D2 and D3 dyes at the optimum values obtained as described before in our previouspaper [13]were mordanted with different mordant by simultaneous mordanting method. Ferrous sulphate, stannous chloride, potassium alumm. sulphate and copper sulphate were used as a metallic mordants.  Substrates Scoured and bleachedwool fabric waspurchased from Misr for Spinning and Weaving Company, Mahalla El-Kobra, Egypt.  Microwave assisted extraction The process ofextraction was carried out by using microwave. A Samsung oven model MS404MADXXBB.  Microwave dyeingmethod Egyptian Journal of Chemistry http://ejchem.journals.ekb.eg/ 353 Morsy Elapasery et.al. _____________________________________________________________________________________________________________ ________________________________________________ Egypt. J. Chem. 64, No. 7 (2021) 3762 The extracted dye were companied with metallic mordant in different concentration and then applied to wool fabrics with M: L ratio 1:100and the dyeing time was 1 hour.  Color measurements Reflectance Spectrophotometer is the device used to measure the intensity of color on dyed wool fabrics andlight reflection technology has been applied for that. The dye yield was determined on the dyed fabric using a spectrophotometer. Kubelka-Munk's Equation (1).Equation was applied to find out the intensity of the color of dye, which is symbolized by the symbol K/S[20]. K/S = [(1R) 2 / 2R] [(1Ro) 2 / 2Ro] (1) Where R is the reflectance of dyed samples, K is the absorption coefficient, S is the scattering coefficient, and Ro = decimal fraction of the reflectance of the undyed fabric.  Fastness properties 1Color fastness to washing The color stability to washing was determined by method of ISO 105-C02:1989 [21]. Aspecimen of the dyed fabric was placed between two bleached slices, one of them is cotton fabric and the other of the wool fabric, and attached with them byhand stitching, and then it was soaked in an aqueous solution consisting of 5 g/L of nonionic detergents at a liquor ratio of 1:50 for 30 minutes at of 60 °C and then sample was rinsed thoroughly with manual squeeze, and then sample was allowed to dry. Gray scale was applied to assess the color fastness to wash. 2Color fastness to perspiration Using L-histidine monohydro-chloride monohydrate (0.5 g), sodium chloride (5 g), and sodium dihydrogen orthophosphate dihydrate (2.2 g) in one liter of distilled water, a solution of artificial sweat was obtained. For have acidic sweat pH was adjusted to 5.5 by 0.1 N of NaOH and by the same way an alkaline sweat was obtained by adjusting pH of solution at 8.0.The fastness test was performed according to the following procedure: Between two different parts of uncolored patterns a sample of dyed fabric (5×4 cm) was sutured. The samples were soaked in both solutions undergoing agitation and pressing for 15-30 min to have perfect wetting. Sample undergo a load of 4-5 kg while the sample was placed between two plates of plastic or glass. Then these plates were placed at a temperature of 37 °C vertically for four hours, and then a gray scale change technique was used to assess the color fastness to perspiration 3Color fastness to light The method of measuring the stability of color fastness to light is ISO 105-B02:1988 test technique where the dyed sample placed for 35 hours to a carbon arc lamp and then using the blue color scale to investigate color change of the tested samples. 4Color fastness to rubbing By applying the technique of ISO 105-X12:1987 test the color fastness to crocking was determined. When dyed fabric undergoes rubbing, it is can be estimate if dye move from dyed fabric to another one or not. The wet and dry rubbing had been estimates. Results and discussion Optimization of mordant concentrations Different concentrations from metallic mordants were applied to dyeing process of wool by D1, D2 and D3 (from 0.02 gm/L to 0.1 gm/L) and then K/S was tested. Data of table 1 and Fig.1 show that the color strength increase by mordant concentration increasing and by using ferrous sulphate as a mordant color shift slightly toward darkness where (L) values decreased and from negative values of (a) and low positive values of (b) color shift from yellow zone to green zone. Stannous chloride gives new dye where (L) values refer that color move to darkness zone and high positive values of (b) low positive values of (a) indicate that dye go to yellow color. In the same behavior potassium alumm. Sulphate has low positive values of (a) and high positive value of (b) then dye found in yellow zone but it becomes darker and that was clear from low positive values of (L). Copper sulphate as a mordant with D1 produced new dye darker than original dye and dye which produced from ferrous sulphate and D1 that was clear from (L) values and negative values of (a) and low positive values of (b) show that dye found in green color zone. Fig. 2 refers that K/S values increased by increasing concentration of metallic mordants. Values of (L), (a) and (b) in table 8 indicate that mixing of ferrous sulphate with D2 color shift slightly toward darkness and color found green zone. Stannous chloride with D2 gives a dye present in darkness zone and go to yellow color due to (L), (a) and (b) values. Combination of Potassium alumm. Sulphate and D2 gives dye has low positive values of (a) and high positive value of (b) then dye found in yellow zone but it becomes darker and that was clear from low positive values of (L). The same behavior of the Copper sulphate as a mordant with D1 is seen when it combined with the D2where new dye is darker than original dye and dye found in green color zone. That is clearly from (L), (a) and (b) values. Fig.3 shows that increasing concentration of metallic mordants when they correlate with D3 leads to increasing in color intensity. MICROWAVE-ASSISTED DYEING OF WOOL FABRICS WITH NATURAL ...... __________________________________________________________________________________________________________________ ________________________________________________ Egypt. J. Chem. 64, No. 7 (2021) 3763 Information of table 9. Show that the selected metallic mordants have the same behavior with D3 when then mixed with it where dye which produced form mixing D3 with ferrous sulphate is dark and found in green zone. Mixture of D3 and stannous chloride produced dye found in dark area and yellow zone. Table 1. Effect of metallic mordant on D1. mordant Mordant conc. K / S L a b c h Without mordant 12.28 64.02 5.04 25.22 25.72 78.70 Ferric sulphate 0.02 9.83 51.52 0.54 10.12 10.13 93.03 0.04 12.35 44.03 0.89 9.76 9.80 95.22 0.06 12.75 45.32 1.24 19.17 9.26 97.69 0.08 13.34 43.33 0.77 10.06 10.09 94.40 0.10 17.85 44.43 1.20 9.02 9.10 97.59 Stannous chloride 0.02 14.85 56.69 2.28 29.84 29.93 85.63 0.04 15.19 52.08 1.71 29.92 29.97 86.73 0.06 16.38 51.40 1.20 29.21 29.23 87.65 0.08 17.98 52.07 0.59 28.14 28.15 88.81 0.10 18.94 52.11 0.49 27.27 27.28 91.03 Pothach. Aluom 0.02 18.31 72.34 6.68 45.37 45.45 86.62 0.04 19.03 71.77 5.25 55.26 55.50 84.57 0.06 19.6 71.29 6.02 58.80 59.10 84.16 0.08 22.10 71.84 6.80 63.86 64.22 83.92 0.10 23.47 72.94 6.27 62.42 62.73 84.27 Copper sulphate 0.02 9.77 69.21 0.04 32.15 32.15 90.07 0.04 10.33 70.01 0.19 33.50 33.50 89.67 0.06 10.65 70.23 0.21 35.46 35.46 89.66 0.08 10.78 71.65 0.02 35.48 35.48 90.04 0.10 13.42 72.06 0.20 33.71 33.71 89.66 Fig. 1. Effect of metallic mordant concentration on D1 Morsy Elapasery et.al. _____________________________________________________________________________________________________________ ________________________________________________ Egypt. J. Chem. 64, No. 7 (2021) 3764 Table 2. Effect of metallic mordant on D2. mordant Mordant conc. K / S L a b c h Without mordant 8.86 65.96 4.59 24.49 24.92 79.3
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