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、XRD和SEM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...     

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。     

Application of polycarboxylic acid sodium salt in the dyeing of cotton fabric with reactive dyes

In this study, the effects of polycarboxylic acid sodium salt on the dyeing of cotton with reactive dyes were evaluated by measuring and comparing the K/S values and dyeing fastnesses of the dyed cotton fabric samples. Results showed that the K/S value and dyeing fastness of cotton fabrics dyed with polycarboxylic acid sodium salt, substituting inorganic salts as exhausting agent were close to that of with sodium chloride when dip‐dyeing process was used. While, in pad‐dry dyeing, the K/S value of cotton fabric samples dyed with polyacid salts as exhausting agent was higher than that of with sodium sulfate, and the dyeing fastnesses of these samples were nearly the same. The dyeing mechanism of cotton fabric with reactive dye, using polycarboxylic acid sodium salt as exhausting agent was analyzed. The dyeing exhausting mechanism of reactive dye seems different when the inorganic salt and polycarboxylic acid sodium salt were used as exhausting agent in the dyeing of cotton fabric with reactive dye. The polycarboxylic acid sodium salt, as weak electrolyte, increased the dye‐uptake of reactive dye on cotton fabric not only by screening negative charges on cotton surface, but also by the effect of salting‐out or hydrophobic combination. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Effects of atmospheric plasma treatment on the dyeability of cotton fabrics by acid dyes

Cotton fabrics were treated with air and argon atmospheric plasma for surface activation. Activated surfaces were grafted with two different amine compounds: ethylenediamine and triethylenetetramine. Pretreated cotton was dyed with acid dye and the effects of pretreatment on the colour strength, as well as the washing, rubbing and the light fastness of the dyeings, were investigated. Colour yield results showed that grafted ethylenediamine and triethylenetetramine enhance the dyeability of cotton fabric with acid dyes. Fourier transform infrared spectra confirmed the formed groups on the surface and scanning electron microscopy showed the etching effect of plasma.     

Durable press finishing of cotton with polycarboxylic acids. II. Ester crosslinking of cotton with dithiosuccinic acid derivative of S-triazine

The preparation of an alternative polycarboxylic acid to replace the most promising but expensive crosslinking reagent butanetetracarboxylic acid (BTCA) was reported in Part I.¹ Part II studies the efficiency of the crosslinking of cotton with the dithiosuccinic acid derivative of s-triazine (HDTST). Diffuse Reflectance infrared (DR FTIR) spectroscopy in combination with wrinkle recovery angle measurements (WRA) were used to analyse the efficiency of cotton cellulose crosslinking. Energy Dispersive X-ray analysis (EDX) of the polycarboxylic acid-finished cotton fabric was performed to study sulphur distribution. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 66: 171–177, 1997     

Chemical modification of cotton to improve fibre dyeability

A new fibre-reactive quaternary compound containing an acrylamide residue was synthesised and used as a cotton modification reagent. The agent was applied to cotton fabrics using a pad-bake process. It was found that the treated fibre could be dyed with reactive dyes without the addition of salt or alkali. The reactive dyes were almost completely exhausted and showed a high degree of covalent bonding with the pretreated cellulose. The effect of varying the pretreatment conditions was investigated and the optimum conditions for pretreating and dyeing were established.     

Modified polyurethane with improvement of acid dye dyeability

This article concerns the modification of polyurethane using polyamide 6,6 prepolymer to improve the dyeability properties of the polyurethane copolymer with acid dye. First, the carboxyl‐terminated polyamide 6,6 prepolymer was synthesized from adipic acid and 1,6‐diaminohexane. The isocyanate‐terminated polyurethane prepolymer was also synthesized from polytetramethylene glycol and 4,4′‐diphenylmethane diisocyanate in N,N‐dimethylformamide. The polyurethane prepolymer was then extended with a mixture of 1,4‐butanediol and the polyamide 6,6 prepolymer (molar ratios of 1,4‐butanediol to prepolymer being 100%, 75%, 50%, and 25%, respectively). Finally, the poly(urethane–amide) copolymers were dyed with acid dyes. The chemical, physical, and the dyeing properties of the poly(urethane–amide) coploymers are discussed. From the experimental results, it is found that the inherent viscosity of poly(urethane–amide) coploymers is increased with the increasing amount of polyamide content. The structure is proven by infrared spectra, which exhibits the absorption peaks of urethane and amide groups as we expected. From the differential scanning calorimetry measurements, it is found that the poly(urethane–amide) coploymers have two‐phase structures and good phase separation. There are four transition temperatures (T_gs, T_gh, T_ms, and T_mh), but only those copolymers in PTMG 2,000 series possess T_ms. Moreover, the T_gs is found to change with the length of soft segment, and the T_gh is increased with the increasing amount of polyamide content. Also, the dyed copolymers exhibit higher T_gh than those without dyeing of dye molecule, but the T_gs is not obviously changed. For mechanical properties, it is indicated that both the modulus and the strength of the coploymers are higher than those of unmodified polyurethane, but they are lowered after being dyed with dye molecule due to further separation of intermolecular distance of the dyed polyurethanes. For dye uptake in dyeing properties, it is found to increase with increasing amount of polyamide content. For dye fastness, the dyed copolymers exhibit higher grade of water fastness than that of unmodified polyurethane. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 1397–1404, 2003     

Pore and crosslinking structures of cotton cellulose crosslinked with DMDHEU‐maleic acid

Two dicarboxylic acids (maleic acid and tartaric acid) were used in conjunction with DMDHEU as the crosslinking agents to treat cotton fabric samples. The treated fabrics then were dyed with direct red 81. The results show that the values of the dye absorption, equilibrium absorption, rate constants, and the pore index of structural diffusion resistance constant for the various crosslinking agents are ranked as DMDHEU‐tartaric acid > DMDHEU‐maleic acid > DMDHEU alone at the same dyeing temperature. The activation energies for the three crosslinked fabrics are in the rank of DMDHEU > DMDHEU‐maleic acid > DMDHEU‐tartaric acid. The CL length values for the various crosslinking agent systems are in the series of DMDHEU‐tartaric acid > DMDHEU‐maleic acid > DMDHEU alone for a given number of CL/AGU. The values of the pore index of structural diffusion resistance constant and dyeing rate constant are increased with the increase of CL length. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 143–148, 2005     

Photoinitiated polymerization of N-methylolacrylamide with crosslinked cotton cellulose

The effects of crosslinking both unswollen and swollen cotton cellulose on the photoinitiated reactions of N-methylolacrylamide (NMA) with cotton are reported. Formaldehyde and dimethylolethyleneurea were used as crosslinking agents. Crosslinked cellulose had a decreased efficiency of photoconversion of NMA to poly(N-methylolacrylamide) (pNMA) with cotton. If the cellulose was crosslinked in the swollen state, increased dosages of ultraviolet radiation gave complete conversion of NMA to pNMA with cotton. Cotton that was crosslinked in the unswollen state probably restricted movement of the aqueous solution of NMA within the fiber and fabric structures and decreased chain propagation within the structures. This restriction resulted in decreased photoconversion of NMA to pNMA with cotton. Transmission and scanning electron microscopy of cotton cellulose that was crosslinked in the swollen state and of cotton cellulose that was crosslinked in the unswollen state showed that swollen cotton was less compacted than unswollen cotton.     

New cationic agents for improving the dyeability of cellulose fibres. Part 2-pretreating cotton with polyepichlorohydrin-amine polymers for improving dyeability with reactive dyes

Pretreatment of cotton with polyepichlorohydrin-dimethylamine produces a modified cotton that can be dyed under neutral conditions with selected low-reactivity dyes using a small amount of salt or with selected high-reactivity dyes without salt. The dyeings of treated cotton exhibit improved colour yield and high wash fastness. The properties and the quality of the reactive dyeings are discussed.     

Physical properties and reaction kinetics of cotton cellulose crosslinked with dimethyloldihydroxyethyleneurea–maleic acid

Two dicarboxylic acids were used to join with dimethyloldihydroxyethyleneurea (DMDHEU) as crosslinking agents to treated cotton fabrics. These results reveal that the dry crease recovery angle values of the treated fabrics for DMDHEU–maleic acid are higher than those for DMDHEU–tartaric acid at a given wet crease recovery angle and tensile strength retention. The IR spectra show that the reaction between the –OH of DMDHEU and cellulose and the vinyl groups of maleic acids occurred. The cross section of the DMDHEU–maleic acid and DMDHEU–tartaric acid treated fibers and the energies of activation and other data of reaction kinetics for DMDHEU–maleic acid and DMDHEU–tartaric acid strongly suggest that the reaction of vinyl groups of maleic acid with cellulose molecules can take place during the pad/dry‐cure process. Additionally, the surface distribution of crosslinking agent on the finished fabrics for DMDHEU–maleic acid is slightly lower than that for DMDHEU–tartaric acid. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 3886–3893, 2004     

Investigation of the improved dyeability of cationised cotton via photografting with UV active cationic monomers

In this study cotton fabric was photografted with cationic monomers using UV radiation. The dyeability of cationised cotton, in the absence of salt, with three classes of dye (direct, reactive and sulphur dyes) was significantly improved due to the increased ionic attraction between the dyes and the cationic cotton. The colour fastness of the cationised fabric was similar or better than that of the untreated fabric. In addition, when cationised, crosslinked crease-resist cotton also showed improved dyeability, in the absence of salt, to direct dyes.     

Modification of cotton to improve its dyeability. Part 1 — pretreating cotton with reactive polyamide-epichlorohydrin resin

Pretreatment of cotton with the polyamide-epichlorohydrin resin Hercosett 125 produces a fibre that may be dyed with selected reactive dyes under neutral pH conditions in the absence of salt and with high fixation efficiency. The physical and mechanical properties of the modified cotton, the colour fastness of the reactive dyeings and mechanistic implications are also discussed.     

New cationic agents for improving the dyeability of cellulose fibres. Part 1 — pretreating cotton with polyepichlorohydrin-amine polymers for improving dyeability with direct dyes

Cotton fibres were treated with polyepichlorohydrin—dimethylamine and dyed with a selection of direct dyes. The pretreatment was found to reduce the amount of sodium chloride needed, and to increase exhaustion efficiency and perspiration fastness. The preparation and chemical characteristics of polyepichlorohydrin-dimetnylamine, the dyeing of the modified cotton and the quality of the direct dyeings are also discussed.     

Durable press finishing of cotton with polycarboxylic acids. I. Preparation of thiosuccinyl-s-triazine

The preparation of an alternative polycarboxylic acid to replace the most promising, but expensive, crosslinking reagent 1,2,3,4-butanetetracarboxylic acid (BTCA) is reported. The reaction of mercaptosuccinic acid with 2,4,6-trichloro-s-triazine (cyanuric chloride) gave a dithiosuccinyl derivative. The preparation reaction was followed using horizontal ATR infrared spectroscopy and capillary electrophoresis. The final product was characterized by FTIR, capillary electrophoresis, and ¹H-NMR. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 66: 1465–1474, 1997     

Process of dyeability modification and bleaching of cotton in a single bath

Graft polymerisation of the cationic monomer, methacryloylaminopropyltrimethylammonium chloride (MAPTAC), onto scoured cellulose was carried out in the bleaching process, aiming at modifying the fibre using a single bath. The extent of MAPTAC fixation on cellulose was measured. The bleaching performance of hydrogen peroxide in the presence of the modifying agent was found to be slightly reduced. The modified bleached cotton fabric was then dyed with a commercial reactive dye in the absence of salt. The dye uptake and colour strength of the modified fabric was markedly increased with an increase in the concentration of MAPTAC. This was attributed to the presence of the cationic groups of the MAPTAC which played a crucial role in attracting the anionic dyes from the dyebath. The results suggest that the dyeing properties of the modified fabric are closely dependent on the efficiency of MAPTAC fixation on cellulose during concurrent modifying and bleaching of cotton.     

Changes in dyeability and morphology of cotton fiber subjected to cellulase treatment

Unprocessed and mercerized cotton fibers were treated with commercial crude cellulase. The changes in the dyeability and structural features of the fiber due to cellulase treatment were studied. The dyeability was examined in terms of uptake of three reactive dyes and the apparent affinity of Congo Red to cotton fiber. The dyeability of the unprocessed fiber was assumed to be influenced by some impurities present in it. This fiber probably resembled polynosic fiber in molecular aggregate at a certain stage of hydrolysis. Mercerized cotton showed a similar pattern in dyeability as weight loss increased, regardless of dye species. Enzyme more easily penetrated the mercerized fiber than the unprocessed fiber. Cellulase treatment influenced the X-ray crystalline reflection pattern for the mercerized fiber but nominally influenced that for unprocessed fiber. Scanning electron micrographs revealed that cellulase treatment caused swelling of the fibrils. They also revealed that the disordered regions between the fibrils in the secondary walls were removed at low weight loss for the unprocessed fiber. The mercerized fiber at high weight loss had large cracks oblique to the fiber axis and showed no individual fibrils in the secondary wall. The primary wall was removed in the initial stage of hydrolysis for both the unprocessed and mercerized fibers. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 65: 155–164, 1997     

Use of chitosan to improve dyeability of DP-finished cotton (II)

Chitosan was used to improve the dyeability of DP-finished cotton. Cotton fabric was treated with a mixture of chitosan, 4,5-dihydroxy-1,3-dimethyl-2-imidazolidinone (DHDMI), and catalyst in a one-step process. To investigate the effect of molecular weight of chitosan on the dyeability of treated fabrics, six chitosan samples of different molecular weights were prepared by depolymerization with sodium nitrite; 185,300, 73,200, 59,000, 21,000, 14,000, and 3,800, respectively. Chitosan improves dye uptake of direct and acid dyes considerably, and the dye uptake increases with the increase of the molecular weight of chitosan. Reactive dye uptake increases slightly in alkaline condition as the molecular weight of chitosan decreases. Higher dye uptake is obtained in acidic condition than in alkaline condition. Chitosan treatment has no discernable effect on the colorfastness to washing, but decreases the colorfastness to wet crocking by about half a point. And chitosan affects other properties of treated fabric; lower wrinkle recovery, stiffer handle, and higher breaking strength as the molecular weight of chitosan increases. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 67:1515–1521, 1998     

Dependence of the dyeability of modified cotton on the substituents and the nature of the dye

Cotton cellulose was chemically modified by introducing acrylamide, acrylonitrile and carboxyalkyl moieties in the form of groups or polymers. In carbamylethylated, cyanoethylated and carboxymethylated cotton, these moieties are in monomeric groups, whereas, in graft copolymers of cotton cellulose with acrylamide, acrylonitrile or acrylic acid, the moieties are in polymeric forms. These substrates were dyed independently using direct, acid, basic or reactive dyes. Results showed that at roughly equal nitrogen content, polyacrylamide–cotton graft copolymer exhibited a much higher colour strength than carbamylethylated cotton when the two substrates were dyed using basic dye. The opposite is the case for direct and reactive dyes. The acid dye produced comparable colour strengths. Similar trends were observed when the other samples were dyed with these four dyes. The results were explained in terms of microstructural changes in the physical and chemical structure of cotton caused by the etherification and grafting reactions.     

Basic dyeability and acid content of high-conversion polyacrylonitrile

Previous data have shown that the basic dyeability of acrylic polymers increases at a given specific viscosity as the peroxydisulfate-to-bisulfite ratio, that is, the catalyst-toactivator (C/A) ratio, is increased. This study represents an effort to understand better the role of the initiator system on the basic dyeability, the acid group composition, and the chain composition of acrylic polymers by preparing model polymers with radioactive initiators. As the C/A ratio is increased, the molecular weight distribution broadens as measured by the M?_v/M?_n ratio, the latter obtained by osmometry. There is also a significant effect of both C/A ratio and molecular weight on the sulfate group content per molecule, but there is no effect of C/A ratio on the number of basic dye sites per molecule, the number of sulfonate groups per molecule, or the weak acid groups per molecule. These effects can be explained by invoking a chain transfer to activator reaction in addition to the usual method of chain termination by recombination. The basic dyeability is found to correlate with the number-average molecular weight and with the number of strong acid groups plus the nonchromophoric weak acid groups.