多元羧酸与指甲醌染料交联染棉的结构及性能

为了提高天然染料对棉纤维的染色固色性能,以聚马来酸（PMA）和柠檬酸（CA）为交联剂应用于天然染料指甲醌对棉织物的交联染色。采用FTIR、SEM和XRD分析了染色前后棉织物的表面形态及结构,探讨了酯交联对棉织物性能的影响以及多元羧酸复配交联染色机理。结果表明,染色前后棉织物表面差别不大,各纤维间不粘连;直接染色后的棉纤维表面变化不明显,仅有少量染料附着,而交联染色后的棉纤维表面负载较多的染料导致其粗糙度增加,酯化反应主要发生在纤维的非晶态区。与直接染色棉织物相比,交联染色棉织物的染色深度（K/S）和上染率分别提高了88%和38%;染品的绿光、黄光增加,颜色饱和度提高;摩擦色牢度提高了1~2级;耐洗色牢度提高了1~2级;交联染色后棉织物的折皱回复角（WRA）提高了约60%,UPF值达到了50+,具有优异的抗紫外性能。     

交联改性壳聚糖在棉织物活性染料染色中的应用

采用交联改性降解壳聚糖对棉织物进行接枝改性,考察壳聚糖接枝改性对棉织物雷马素活性染料染色性能的影响.结果表明:棉织物经壳聚糖改性后,增加了织物表面对染料阴离子的亲和力和固着力,上染率和K/S值都有所提升,其固色率也有很大提高,均达80%以上;经雷马素红RR和雷马素黄RR染色后,改性棉织物的干、湿摩擦牢度和耐皂洗褪色同未改性棉织物一样,分别为4、3~4和4级,耐皂洗沾色降低半级,为3~4级.用雷马素蓝RR染色后,改性棉织物干摩擦牢度提高半级,达4级,湿摩擦牢度和耐皂洗等级同未改性棉织物一样,分别为3~4和4级.     

多元羧酸复配提升1,4-萘醌天然染料对棉的染色性能

为改善1,4-萘醌天然染料对棉织物的染色性能,采用柠檬酸与酒石酸复配进行交联染色。采用扫描电镜、红外光谱分析了染色前后棉织物的结构,探讨了染色前后棉织物的染色性能和物理性能以及染色机理。结果表明,交联染色后,1,4-萘醌天然染料通过酯键固着在织物上,棉织物表面变得粗糙。与1,4-萘醌天然染料直接染色样品相比,采用柠檬酸和酒石酸复配交联染色后染品的上染率和染色深度(K/S)分别提高了21%和83%,匀染性良好,染品的黄光增加,颜色饱和度提高,摩擦牢度提高了1～3级,耐洗色牢度提高了1～2级,抗皱性能大约提高了50%,水接触角提高了11%。     

Atmospheric pressure plasma‐induced decolorisation of cotton knitted fabric dyed with reactive dye

The aim of this study was to investigate the decolorisation effect of atmospheric pressure plasma treatment on knitted fabrics dyed with reactive dyes under different processing parameters, ie, air concentration, treatment duration and water content. The fabrics were dyed with reactive dye of a blue colour, and the colour depths were 0.5%, 1.5% and 3.0% on weight of fabric. The colour properties of untreated and plasma‐treated fabric samples were evaluated by means of reflectance, K/S and relative unlevelness index. The colour properties were evaluated instrumentally and quantitatively in order to study the decolorisation effect induced by atmospheric pressure plasma treatment. Experimental results revealed that the desired decolorisation effect was heavily influenced by the atmospheric pressure plasma treatment processing parameters. Although the desired decolorisation effect could be obtained by controlling the processing parameters of the atmospheric pressure plasma treatment, the treatment did not provide any significant reduction in the bursting strength of the fabric.     

Optimal dyeing systems for resistance to the physical strength loss of the PLA/cotton blended fabric

In this study, optimization of disperse/reactive dyeing systems for resistance to the physical strength loss of Poly(lactic acid) (PLA)/cotton blended fabric was investigated. The blended fabric underwent a two‐bath, two‐stage dyeing process in which the PLA component of the blended fabric was dyed using two disperse dyes, followed by the cotton component being dyed with six reactive dyes containing different reactive groups—dichlorotriazine, monochlorotriazine, sulphatoethylsulphone, monofluorotriazine, monochlorotriazine/sulphatoethylsulphone, and monofluorotriazine/sulphatoethylsulphone groups. The optimal dyeing systems were established according to the fixation rate of the dyes, tear/tensile strength loss, and SEM micrographs of the fabric. To avoid the strength loss during the disperse/reactive dyeing process, the recommended disperse dyeing conditions were 110°C, pH 5 for 20 min, whereas the reactive dyeing conditions should be temperature ≤60°C and alkali concentration ≤3 g/L. In this regard, reactive dyes containing monofluorotriazine and monofluorotriazine/sulphatoethylsulphone groups were especially suitable for the reactive dyeing systems. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Alkaline dyeing of polyester and polyester/cotton blend fabrics using sodium edetate

An alkaline dyeing of polyester with an alkali‐stable disperse dye, Dianix® Scarlet AD‐RG, was developed using sodium edetate as an alkaline buffering agent. The results obtained indicate the suitability of using sodium edetate for alkaline dyeing of polyester when compared with the control alkaline dyeing using Dianix AD system. Selected mono and bifunctional reactive dyes were used in combination with the alkali‐stable disperse dye for dyeing of polyester/cotton blend. Different dyeing methods for cotton and polyester/cotton blend fabrics using sodium edetate were evaluated in comparison with their respective control alkaline dyeing methods. The results of using sodium edetate in one‐bath two‐stage and two‐bath dyeing of polyester/cotton blend were comparable with that of the control dyeing method. Particularly, no change in the leveling and fastness properties was evaluated for all samples irrespective of the dyeing method. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

棉织物漂染废水的污染预测

为明确棉织物漂染废水中污染物的组分,采用m(BOD5)/m(CODCr)法测试了常用染料和助剂的可生化性,按实际漂染工艺和配方对棉织物进行前处理、染色和柔软处理,收集各阶段试验废水并进行分析。研究结果表明,棉织物漂染废水的CODCr主要由各种难降解的助剂和棉织物上的有机物所组成,其中各种难降解助剂的CODCr占废水总CODCr的63.3%,残余染料造成的色度高达800倍,柔软剂的CODCr在漂染废水总CODCr中所占的比例最大,约为57.5%。     

Possibilities of polymer‐aided dyeing of cotton fabric with reactive dyes at neutral pH

Water‐soluble polymers have versatile application, viz., water‐soluble polyacrylates have been widely used in the reactive dyeing of cellulosic fibers and the related soaping as an important component of the leveling and washing agent. In this article, one such water‐soluble polymer, polyacrylic acid has been synthesized, characterized, and applied in conjunction with various types of reactive dyes, namely triazinyl, vinyl sulfone, high exhaustion, and bifunctional reactive dyes, along with crosslinking agents, namely glycerol 1,3‐dichlorohydrin and hexamethylene tetramine‐hydroquinone, respectively. One of the crosslinking agents (the former one) has been synthesized in the laboratory. Crosslinking agent is necessary to adhere the dye molecule onto the cellulose macromolecule. Different process sequences have been formulated and explored for dyeing purpose. All such dyeings were carried out at neutral pH. The dyed samples were assessed through color strength in terms of K/S values and their fastness properties were assessed by standard methods. All such dyeings were compared with conventional dyed samples. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Ultrasonic‐assisted dyeing: II. Nylon fibre structure and comparative dyeing rate with reactive dyes

Comparative dyeing kinetics of nylon‐6 fibre with different reactive dyes using conventional and ultrasonic conditions are presented. The time/dye‐uptake isotherms are revealing the enhanced dye‐uptake in the second phase of dyeing (diffusion phase). The data of dyeing rate fit well with the integrated form of the first‐order rate equation and values of dyeing rate constant and half‐time of dyeing are discussed. Ultrasonic efficiency in accelerating the dyeing rate relative to conventional heating was examined for all dyes used to show that ultrasonics are most effective for a dyeing system which has difficulty in achieving high dye‐uptake. To clarify the role of fibre fine structure and whether it is affected during dyeing with ultrasonic waves, time‐dependent ultrasonic pre‐treatment of nylon‐6 fibres and its effect on the colour strength obtained is presented. X‐ray diffraction studies on nylon‐6 fibres conventionally and ultrasonically pre‐treated have shown that the percentage of fibre crystallinity has become higher in ultrasonically treated fibre in comparison with that of conventionally treated. Although the increased crystallinity of the fibre, which occurs simultaneously during the ultrasonic dyeing process, would retard dye uptake, it seems that the enhanced effect of power ultrasonic is high enough to overcome this side‐effect on the fibre. © 2003 Society of Chemical Industry     

纳米分散染料胶囊的制备及其对涤纶织物轧染染色性能

针对涤纶织物浸轧染色存在浮色多、后水洗负担重的问题，通过乳液聚合法制备了以分散染料为核，甲基丙烯酸甲酯（MMA）-丙烯酸丁酯（BA）共聚物为壳的纳米分散染料胶囊（NDDM），探究了核壳投料比、软硬单体配比、固色温度和固色时间等因素对涤纶织物轧染染色性能的影响。结果表明，NDDM对涤纶织物轧染染色的色牢度和匀染性均优于C.I.分散紫93染色织物，当核壳质量投料比为1:2、MMA和BA质量投料比为1:1，焙烘温度180 ℃、焙烘时间5 min时，NDDM轧染染色织物的颜色深，手感变化小，且未水洗染色织物的各项色牢度达到4级及以上，还原清洗COD值为312.3 mg/L，COD值较C.I.分散紫93染色相比下降了58%。在高温条件下，NDDM内分散染料从聚丙烯酸酯壳层内迁移释放并上染纤维，聚丙烯酸酯壳将未进入纤维内的残余染料覆盖固着在纤维表面。     

Salt-free reactive dyeing of betaine-modified cationic cotton fabrics with enhanced dye fixation

Novel cationic cotton fabrics were prepared by an efficient and simple one-step pad–dry–bake pretreatment process with betaine as cationic reagent. Ester bonds formed between cotton fibers and betaine hydrochloride were proved by Fourier transformed infrared attenuated total reflection(FTIR-ATR) spectra. Moreover, the properties of the cationic fabrics, including X-ray Diffraction(XRD), tensile strength and whiteness and yellowness index,were investigated in comparison with that of the untreated ones. The cationic fabrics were applied in salt-free dyeing of C.I. Reactive Red 195, C.I. Reactive Yellow 145 and C.I. Reactive Blue 19. Different dye fixation processes were applied and compared for untreated and cationic cotton. Dye fixation and color fastness properties of the dyes were tested, and the results presented that dye fixation on the cationic fabrics in the absence of salt was improved with satisfactory light fastness property and applicable wash and rub fastnesses.     

Dye–fibre bond stabilities of some reactive dyes on cotton

Cotton fabric dyed with commercial reactive dyes of the monochloro-s-triazine, bis(monochloro-s-triazine), and bis(monofluoro-s-triazine) type was treated in buffer solutions pH 10 and 12 at 60, 85 and 98°C. Hydrolysis has been investigated using spectrophotometrical measurements of hydrolysed dye at λ_max. The percent of hydrolysed dye was calculated.     

Pigment dyeing of polyamide‐epichlorohydrin cationized cotton fabrics

A synthesized cationic reagent named polyamide‐epichlorohydrin (PAE) was used to cationize cotton fabrics which were dyed with nanoscale pigments after PAE modification. The results showed that when the PAE concentration was below 7% (owf), the K/S value increased nearly linearly with increasing of PAE concentration, and excess that concentration the K/S value did not increase further. With increasing the pH value of cationization bath, the K/S value increased first and then decreased, the maximum K/S value appeared at pH 9–10. Cotton fabrics cationized at 80°C for 20 min exhibited the best cationizing result. Both the pigment uptake and the color strength reached their own maximum values when the dye bath was neutral. When the pigment concentration was 1% (owf) the addition of 1g/L sodium chloride in the dye bath could decrease the pigment uptake while for 5% (owf) pigment concentration the uptake increased with increasing the amount of sodium chloride. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

IR spectroscopy study of cyclic anhydride as intermediate for ester crosslinking of cotton cellulose by polycarboxylic acids. V. Comparison of 1,2,4-butanetricarboxylic acid and 1,2,3-propanetricarboxylic acid

In recent years extensive efforts have been made to use multifunctional carboxylic acids as formaldehyde-free crosslinking agents for cotton to replace the traditional formaldehyde-based N-methylol reagents. In our previous research we found that a polycarboxylic acid esterifies cellulose through the formation of a five-membered cyclic anhydride intermediate by dehydration of two adjacent carboxyl groups. In this research we used Fourier transform IR (FTIR) spectroscopy to study the formation of cyclic anhydride intermediates and crosslinking of cotton by 1,2,4-butanetricarboxylic acid (BTA) and 1,2,3-propanetricarboxylic acid (PCA). BTA and PCA form five-membered cyclic anhydrides in the same temperature range. Both acids form the anhydrides at lower temperatures when a catalyst is present. When an acid molecule is bonded to cotton through an ester linkage, only PCA is able to form a second anhydride intermediate. We found that PCA is a more effective crosslinking agent, and it imparts higher levels of wrinkle resistance to the cotton fabric than BTA. Therefore, the formation of a five-membered cyclic anhydride by a polycarboxylic acid accelerates the esterification of cotton by the acid. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 2142–2150, 2001     

Optimization of cotton crosslinking with polycarboxylic acids and nano TiO2 using central composite design

The cotton crosslinking with butane tetra carboxylic acid (BTCA) and citric acid (CA) in the presence of sodium hypophosphite (SHP) and nano TiO₂ (NTO) under different curing conditions were optimized using a statistical model. The central composite design (CCD) was used for variables based on Design of Expert software. The appropriate model to create optimum crease recovery angle was obtained for each condition. The X‐ray diffraction (XRD) and scanning electron microscopy (SEM) were also employed to indicate the NTO particles on the fabric surface with the size of nano particles and their crystallinity. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

季铵型阳离子聚丙烯酰胺的无盐染色行为

以季铵型阳离子聚丙烯酰胺作为一种新的阳离子助剂对棉纤维进行处理,应用于活性染料无盐染色,对染色过程中染料与处理后棉纤维之间的吸附类型、吸附热力学及吸附动力学进行了研究。结果表明,无盐染色过程符合Langmuir吸附模型;吸附过程是放热自发进行的,低温有利于染料的吸附;吸附动力学符合二级动力学模型,属于化学吸附过程。与传统有盐染色结果相比,染色后的阳离子化棉纤维色深增加,染料利用率提高。     

Synthesis and characteristics of aqueous reactive urethane oligomer containing sulfoisophthalate sodium salt

This research studied urethane oligomers, which contains the sulfonic acid group and different reactive groups. First, the transesterification of dimethyl 5‐sulfoisophthalate sodium salt were performed with ethylene glycol or polyethylene glycol of different molecular weights to produce PEG soft chains possessing sulfonic acid group. Subsequently, isophorone diisocyanate used as a hard chain was connected to the two terminals of the sulfonated diols, which finally were blocked by methyl ethyl ketoxime or hydroxyethyl methacrylate or 2, 3‐Epoxy‐1‐propanol to form three kinds of aqueous reactive urethane oligomers (MSE, HSE, and OSE). The MSE oligomer had the greatest particle diameter, particle variance, and streaming current readings; the HSE oligomer, and the OSE oligomer had the second large and the smallest readings of the aforementioned measurements, respectively; whereas the contact angle and surface tension appeared with an opposite trend. Within the thermal properties of oligomer, the T_g of oligomer followed the trend: OSE < HSE < MSE; however, T_m and ΔH show an opposite tendency. With regard to the reactivity of the oligomers toward PET fabric, the add‐on for the variety of oligomers was in the quantity order of MSE > HSE > OSE series, and the washing durability was rated in the order of HSE > MSE > OSE series. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Ultrasonic‐assisted dyeing: I. Nylon dyeability with reactive dyes

The use of ultrasonic power (38.5 KHz, 350 W) to assist the dyeability of nylon‐6 fibre with reactive dyes is reported. The effects of the different factors that may affect the dyeability of nylon‐6 fibre with Reactive Red 55 were simultaneously carried out under both ultrasonic power and conventional heating conditions. The colour strength values obtained for the dyed samples using ultrasonic power were higher than those obtained using conventional heating. Also, the effect of alkaline soaping treatment on dye fixation for the dyed fabrics with different reactive dyes, at both acidic and neutral pHs, is generally better with ultrasonic than with conventional heating. The overall results indicate that the enhancing effect is mainly attributed to the de‐aggregation of dye molecules, which leads to better dye diffusion and possible assistance for dye‐fibre covalent‐bond fixation. The results of wet fastness properties of the dyed fabrics reveal improvement using ultrasonic power dyeing relative to the conventional heating method. © 2003 Society of Chemical Industry     

HN-型高固色率活性染料的低盐染色法

HN-型高固色率活性染料红HN-2B、金黄HN-R、深蓝HN-2G,其吸色率在95％以上,固色率在85％左右。以几种不同的染色方法,用HN-型高固色率活性染料对棉纱及棉布进行了染色,染色结果表明,在中温下,该活性染料可以采用低盐染色。当盐的加入量减少为30g/L是标准加入量的1/2）,其最适宜的染色条件为:浴比1∶20,染色深度3％,40℃上染,60℃固色,氯化钾20g/L和柠檬酸三钠为10g/L,碱磷酸三钠的加入量为4+10g/L时,其K/S值下降百分数:红HN-2B为10.16;金黄HN-R为5.57;深蓝HN-2G为8.57。     

Physico-chemical modelling of the dyeing of cotton with reactive dyes

Over the past decades a great deal of research effort has been devoted to understanding the physico-chemical mechanism of the dyeing of cotton with reactive dyes. However, the use of physico-chemical models has been almost exclusively restricted to research laboratories due to the simplifying assumptions used. A more practical model has now been developed and is intended to allow dyeing recipes and the process parameters used in bulk production to be optimised. The model is additionally able to quantify the effect of non-controllable variables on overall dyeing efficiency.