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.     

高阳离子化度叔胺型聚丙烯酰胺在活性染料无盐染色中的应用(英文)

Tertiary amine cationic polyacrylamide with high cationization degree was used as a new cationic agent to pretreat cotton with dip-pad-bake method. The obtained cationic cotton was dyed with reactive dyes in the absence of electrolyte. The effects of the characteristics of the cationic agent and the pretreatment conditions on dyeability of reactive dye were investigated. The results showed that the fixation and K/S values of the reactive dyes on the cationic cotton were improved compared with those on the un-treated one in the presence of salt. Tests on fastness properties of the dyed cotton and fabric quality of the pretreated cotton were carried out and the results showed that wash and rub fastness of the salt-free dyeing were both satisfactory. And anti-crease property, tensile and tear strength, and handling of the cationic cotton were also good compared with that of the untreated one.     

超临界流体抗溶剂法制备叶黄素/羟丙甲纤维素邻苯二甲酸酯纳米微胶囊

Lutein was nano-encapsuled with hydroxypropylmethyl cellulose phthalate (HPMCP) to maintain its bioactivity and to avoid thermal/light degradation. Supercritical antisolvent precipitation was applied to prepare lutein/HPMCP nano-capsule. The effects of several operating parameters on the yield, lutein loading, encapsulation efficiency, particle size and particle size distribution of the nanocapsule were investigated. The mean diameter of nanocapsules ranged from 163 nm to 219 nm under appropriate experimental conditions. The result of scanning electron microscope showed that the nanocapsules were nearly spherical. The highest yield reached 95.35% when the initial concentration of lutein was saturated. The highest lutein loading of 15.80% and encapsulation efficiency of 88.41% were obtained under the conditions of 11 MPa, 40C and CHPMCP︰Clutein 5︰l. The results may pro-mote the application of lutein in food industry.     

壳聚糖/乙基纤维素微胶囊的制备及特性

In this work a system which consists of chitosan microcores entrapped in ethylcellulose is presented.Vitamin D2 was eficiently entrapped in chitosan microcores with spray-drying method and was microencapsulated by coating of ethylcellulose.The average size of chitosan microspheres was 6.06μm.The morphology and release properties of microcapsules were tested.The results of release in vitro showed that the microcapsule could realize sustained release for 12h in artificial intestinal juice.     

The combined effects of lysozyme and ascorbic acid on microstructure and properties of zein-based films

Edible zein-based films containing lysozyme(LY) and ascorbic acid(AA) were developed in the presence of polyethylene glycol 400(PEG 400), the combined effects of LY and AA on the microstructure, mechanical properties and release properties of developed zein films were investigated in detail. The results of microstructure characterization indicated that zein-based films became compact and smooth, and LY aggregates were well distributed in the zein matrix because of the simultaneous addition of LY and AA. The results of mechanical tests showed that because of the synergistic effects of LY and AA on zein film, elongation at break of zein-based film could be up to 138%, which was 34.5 times higher than that of zein control film. LY release tests showed that when the concentration of AA was less than 3.1 mg·cm~(-2), the release rate of LY significantly decreased by 33.7%, and the total release increased by 80.6%. While the release profiles of AA showed that the release rate and total release of AA from the films containing LY increased by approximately 68.9% and 61.7% than the films without LY. Good antioxidant and sustained antimicrobial activities were found for the developed zein films.     

载三氧化二砷的PEG—PLGA隐性纳米粒的制备及体外研究

The aim of this study was to prepare arsenic trioxide （ATO）-loaded stealth PEGylated PLGA nanoparticles （PEG-PLGA-NPs） and to assess the merits of PEG-PLGA-NPs as drug carriers for ATO delivery. PEG-PLGA copolymer was synthesized with methoxypolyethyleneglycol （Mw=5000）, D, L-lactide, and glycolide by the ring-opening polymerization method. Amorphous ATO was transformed into cubic crystal form to increase its solu-bility in the organic solvent. ATO-loaded PEG-PLGA-NPs were prepared by the modified spontaneous emulsification solvent diffusion （SESD） method, and the main experimental factors influencing the characteristics of nanopar- ticles were investigated, to optimize the preparation. To confirm the escape of PEG-PLGA-NPs from phagocytosis by phagocytes, PEG-PLGA-NPs labeled rhodamine B uptake by murine peritoneal macrophages （MPM） were analyzed by flow cytometry. The results showed that the physicochemical characteristics of PEG-PLGA-NPs were affected by the type and concentration of the emulsifiers, polymer concentration, and drug concentration. ATO-loaded PEG-PLGA-NPs, with particle size of 120.8nm, zeta potential of-10.73mV, encapsulation efficiency of 73.6%, and drug loading of 1.36%, were prepared under optimal conditions. The images of transmission electron micros-copy （TEM） indicated that the optimized nanoparticles were near spherical and without aggregation or adhesion. The release experiments in vitro showed the ATO release from PEG-PLGA-NPs exhibited consequently sustained release for more than 26d, which was in accordance with Higuchi equation. The uptake of PEG-PLGA-NPs by MPM was found to decrease markedly compared to PLGA-NPs. The experimental results showed that PEG-PLGA-NPs were potential nano drug delivery carriers for ATO.     

一种新颖的含黄酮结构可交联高分子染料的合成与染色性能研究(英文)

A yellow crosslinking polymeric dye was prepared by grafting the flavone moiety containing azo chromophore onto polyvinylamine backbone.The λ max of this polymeric dye in water is 382 nm.The polymeric dye is fixed to silk and cotton with a crosslinking agent,2-chloro-4,6-di(aminobenzene-4’-β-sulphatoethylsulphone)-1,3,5-s-triazine,which acts as a bridge between the fiber and dye molecules.The fixation of this polymeric dye reaches 99% and the dyed samples exhibit excellent rubbing and washing fastness.     

载5-氟尿嘧啶的pH敏感自组装纳米粒制备及体外释放

In order to improve the cancer-targeting and selective activity of antineoplastic agent [5-fluorouracil （5-FU）], a novel pH-responsive drug delivery system [pullulan acetate/sulfonamide （PA/SDM） conjugate] was synthesized by a diafiltration method. Sulfonamide was grafted to the hydrophobicaUy modified pullulan acetate to enhance the pH sensitivity for better cancer-targeting delivery. 5-FU was loaded into the self-assembled nanoparticles by the same method. The drug-loaded self-assembled nanoparticles were successfully obtained and characterized in terms of particle size, morphology and drug loading and release profile at various pHs. The results showed that the mean diameter of the self-assembled particles was approximately 100nm, with uniform size and good spherical morphology. The nanoparticles showed good stability at pH 7.4, which is equal to that of the normal body fluid, but shrank and aggregated below pH 6.8, which is close to the pH with tumors. The loading efficiency and concentration of released 5-FU was monitored at 269 nm on the UVNis spectrophotometer. The release profile was heavily pH-dependent around phvsiological pH, and the release rate was significantly enhanced under pH of 6.8.     

EFFECT OF Ni CRYSTAL SIZE DISTRIBUTION ON THE ANTICOKING BEHAVIOR OF La-MODIFIED Ni/α-Al_2O_3 CATALYSTS

The crystal size distribution(CSD)was determined with small angle X-ray scattering technique.Theanticoking property of Ni-catalysts was investigated with the steam reforming of n-heptane in a TG-monitoredflow reactor.The results of this study show that the rate of coking on the supported Ni-catalysts depends main-ly on the percentage content of the large size fraction(25-70nm)of Ni-crystallites,and that the dispersion ofNi-crystallites and the anticoking property of the Ni/α-Al_2O_3 catalysts were promoted obviously by theLa_2O_3-modification method.The variation of the Ni-CSD and the anticoking property of the catalysts were fur-ther tested through different periods of hydrothermal treatment.It is found that the content of the largeNi-crystal size fraction and the coking rate pass correspondingly through a maximum.     

氟脲嘧啶微粒-壳聚糖微敏性水凝胶复合释药系统的制备

The auto-gelling and drug release properties of the thermosensitive chitosan-β-glycerophosphate formulation were investigated. According to rheological study, gelation lag time of chitosan/β-glycerophosphate （GP） solutions varied from 2 to 60min with different deacetylation degree of chitosan, pH, gelation temperature, and the particles in the sol. The gelation properties were also found to influence the release profilles of a hydrophilic drug, 5-fluorouracil （5-FU）. Morphological examination by scanning electron microphotography demonstrated that large ＂pores＂ occurred during the gel-forming process, which created hydrophilic environment and led to the rapid initial release of the drug （85% in f＇LrSt 8h）. Poly-3-hydroxybutyrate （PHB）, a biodegradable material, was applied here as scaffold to capture 5-FU into microparticles with high encapsulation efficiency by solvent-nonsolvent method. Combination of these microparticles into the chitosan-β-GP formulation could drop the rapid initial release from 85% down to 29% in the optimized PHB content （75%, by mass）. The release could sustain for about 10 months. Tiffs study provided an understanding of the potential of injectable implant using thermosensitive chitosan-β-GP formulation containing PHB based particles for the water soluble drugs that need the property of long-term delivery.     

Properties of osmanthus fragrance‐loaded chitosan–sodium tripolyphosphate nanoparticles delivered through cotton fabrics

Osmanthus fragrance‐loaded chitosan nanoparticles (OF‐NPs) were prepared via complex coacervation successfully. Then, the OF‐NPs were applied in the cotton fabrics directly. The microstructures of OF‐NPs were characterized by dynamic light scattering (DLS), transmission electron microscopy (TEM), Fourier transformation infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA). The sustained property of the cotton fabrics treated with OF‐NPs was investigated with scanning electron microscopy (SEM) and gas chromatography‐mass spectrometry (GC‐MS). The common OF was also treated on fabrics for the parallel comparison. TEM and DLS displayed that the spherical OF‐NPs kept about 130 nm and dispersed evenly. FTIR confirmed that OF had been interacted with chitosan via the hydrogen bonds. TGA demonstrated that the thermal stability of OF‐NPs had been improved in contrast to OF and the loading content of OF was as high as 12.05%. SEM and GC‐MS displayed that the cotton fabrics treated by OF‐NPs had an excellent washing resistance. Overall, nanoencapsulation with CS‐TPP will provide an excellent method for releasing fragrance. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Synthesis and application of polyacrylate nanocapsules loaded with lilial

Polyacrylate nanocapsules loaded with lilial (PNLs) were prepared via miniemulsion polymerization. Then, the PNLs were applied directly to leather. The influence of the contents of the surfactant and lilial and the stirring speed on the mean size and fragrance loading capacity of the PNLs was investigated in detail. The microstructure of the PNLs was determined by dynamic light scattering (DLS), transmission electron nicroscopy (TEM), Fourier transform infrared (FTIR) spectrometry, and thermogravimetric analysis (TGA). The sustained release properties of the leather finished by PNLs were characterized by scanning electron microscopy (SEM) and gas chromatography with a flame ionization detector (GC‐FID). DLS showed that the mean size of the PNLs was 67.78 nm, and the polydispersity index was 0.076. TEM illustrated that the size of the spherical PNL varied in the range 30–80 nm. FTIR spectroscopy showed that lilial was encapsulated into the polyacrylate nanocapsules. TGA illustrated that the fragrance loading ratio of the nanocapsules reached 36.83%. SEM and GC‐FID indicated that the leather finished by the PNLs had better flexing endurance than that finished by lilial emulsion. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40182.     

Sustained‐release properties of cotton fabrics impregnated with nanotuberose fragrance

Tuberose‐fragrance (TF) loaded polybutylcyanoacrylate nanoparticles were successfully prepared via emulsion polymerization. The nanotuberose fragrance (Nano‐TF) was directly impregnated into the cotton fabrics as an aromatic reagent. Dynamic light scattering and transmission electron microscopy showed that the average size of the spherical Nano‐TF was 202.4 nm. Fourier transform infrared spectroscopy demonstrated that TF was encapsulated into the BCA nanoparticles and that the Nano‐TF was in existence in the cotton fabrics. Thermogravimetric analysis showed that the loading TF content of the Nano‐TF was 50.9% and that 10.02% Nano‐TF had been impregnated into the fabrics. A lot of Nano‐TF was adhered onto the surface of the cotton fabrics after 50 washings, as shown by scanning electron microscopy and gas chromatography/hydrogen flame ionization detection (GC–FID). In addition, GC–FID demonstrated that most aroma compounds of the cotton fabrics impregnated with Nano‐TF only lost less than 20% of their aroma after 60 days of deposition and around 75% of their aroma after 6 h of deposition at 120°C, so they showed better sustained‐release properties than those with TF. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41678.     

植酸对羽毛角蛋白整理涤纶织物性能的影响及分析

为提高羽毛角蛋白（FK）对涤纶织物的后整理效果及其耐久性，本文向羽毛角蛋白整理液中添加了植酸（PA）组分，采用SEM和FTIR对整理前后涤纶织物的形貌和结构进行了表征，同时比分析了PA对FK整理涤纶织物表面静态接触角、芯吸高度、抗静电性能的影响规律。此外，将整理的涤纶织物进行洗涤处理，测试了织物上FK的保留率。结果表明：与单一组分FK整理的涤纶织物相比，PA组分的加入使得涤纶织物表面的FK附着量增加，整理涤纶织物的芯吸高度与抗静电性提升，表面静态接触角下降；同时PA还提升了FK整理涤纶织物的耐久性，经相同工艺水洗后，具有较高的FK保留率。     

抗紫外聚多巴胺香料纳米胶囊缓释体系的研究

利用多巴胺(DA)在碱性溶液中的自氧化和聚合,在香料乳液液滴表面涂覆聚多巴胺(PDA)层制备香料PDA纳米胶囊,比较了PDA对不同香料的包覆性能和缓释效果。结果发现苯乙醛和香茅醛因与多巴胺(DA)发生Maillard反应而不能被包覆,苯乙醇、香茅醇、乙酸苯乙酯和乙酸香茅酯则能被包覆在纳米胶囊内部,扫描电子显微镜(SEM)和动态激光光散射(DLS)结果显示:香料纳米胶囊基本呈球形,分布较均匀,香料种类对粒径影响大,可由88 nm(乙酸香茅酯)变化到556 nm(苯乙醇)。对香茅醇的包埋率最高,可达到19. 8%,在常温下保存50 d后香料保留率可保持69. 39%以上,具有良好的缓释性能,同时由于PDA对紫外及可见光有一定的吸收,因此可以为光敏性或光毒性香料的应用提供进一步的光屏蔽作用。     

A quantitative study of factors that influence the substantivity of fragrance chemicals on laundered and dried fabrics

Model investigations of physicochemical aspects of the substantivity of fragrance raw materials on laundered fabrics were performed. The overall process was divided into two consecutive steps, laundry and dryout, which were characterized by affinity and tenacity, respectively. The affinities of fifteen fragrance raw materials to cotton and polyacrylonitrile were measured in standard fabric softener and detergent solutions. Affinities correlated with the corresponding partition coefficient, P(o/w). To study the impact of parameters independent of the chemical structure of the fragrance molecules, 1-[³H]-3-methyl-5-phenylpentanol (phenylhexanol) was selected, and aqueous solutions of defined anionic, nonionic and cationic surfactants were used as model detergent and fabric softener media. A sequence of experiments, based on the fractional factorial design, was planted for quantifying the relative contribution on substantivity of a number of variables: the concentration of the fragrance chemical, the type and concentration of the surfactants, the type and weight of the fabrics (cotton or polyacrylonitrile) and the washing temperature in the case of cotton. The affinity that characterizes the washing process depends mainly on the type of fabric and the type of surfactant and, to a lesser extent, on the surfactant concentration and the temperature. Anionic and nonionic surfactants, the main components of detergent powders, behave similarly, whereas the combination of cationic surfactant with cotton markedly enhances the affinity. For phenylhexanol, the tenacity after dryout is largely controlled by the type of fabric. The role of fiber swelling is discussed. The substantivity, which represents the global effect of laundering and dryout, shows the same trend as the affinity. The complexity of the physicochemical phenomena involved is highlighted by the importance of the interactions between the main contributing factors.     

Property modifications of finished textiles by a cationic surfactant

Fabrics made of 100% cotton, 100% polyester and a 50/50 cotton/polyester blend with and without functional finishes were treated in aqueous solutions of the cationic surfactant distearyldimethylammonium bromide (DSDMAB). Finishes chosen were dimethyloldihydroxyethyleneurea (DMDHEU), a durable press finish, and poly(acrylic acid), a soil release finish. Selective sorption of the cationic surfactant by finished and unfinished fabrics was quantified. Cotton takes up much larger amounts of DSDMAB than does polyester. In general, acrylic finished fabrics take up more DSDMAB, while DMDHEU finished fabrics take up smaller amounts of DSDMAB as compared to their unfinished controls. These findings indicate that ionic interaction forces play an important role in the sorption process. In order to investigate this, acid numbers were used as a relative measure of negative sorption sites on fabrics. A direct relationship between DSDMAB sorption and the acid numbers of the fabrics was established. Perceived fabric softness is generally improved by treatments with DSDMAB for all test fabrics. Although cotton fabrics finished with DMDHEU were perceived to be less soft than unfinished cotton, treatment with DSDMAB restored the softness level to that of unfinished cotton. The softness of both cotton and polyester fabrics was greatly lowered by the acrylic finish. The presence of even large amounts of DSDMAB did not restore softness ratings to levels comparable to unfinished controls. Electrical resistivity and electrostatic clinging measurements were used to assess the effectiveness of DSDMAB as an antistatic agent. DSDMAB reduced the electrical resistivities of all test fabrics. However, relative humidity played a much larger role in reducting the electrical resistivity of fabrics. Clinging times were also reduced by DSDMAB treatments. DSDMAB was particularly efficient in reducing the clinging time of polyester. Additional moisture related properties were investigated. The presence of DSDMAB on the test fabrics did not significantly alter moisture regain. The application of DSDMAB from aqueous solutions resulted in lower water retention values of the test fabrics after centrifuging at ag-factor comparable to home washing machines. This leads to energy savings during drying from 10–24%, depending on the fabric and finish type. However, energy savings due to fiber type were more significant than those due to the cationic surfactant treatment.     

棉织物的纳米银多功能整理

以植物还原剂——金银花提取物和化学还原剂——丙三醇,分别还原硝酸银,制备了两种纳米银溶液。采用浸渍法将上述制备的纳米银溶液分别对棉织物进行功能整理。利用SEM、EDS、XRD、FTIR分析整理前后棉织物的外观形貌及结构,并探讨了整理后的棉织物的抗紫外性能、不同洗涤次数后其含银量、色差和抗菌性能的变化。结果表明,纳米银粒子主要通过范德华力吸附在棉织物纤维素的无定形区;与化学还原法相比,植物还原法制备的纳米银粒径减小了约15nm,植物还原法制备的纳米银溶液整理后的棉织物经过50次洗涤后,棉织物表面的纳米银吸附量及色差变化不大,且对大肠杆菌和金黄色葡萄球菌的抑菌率仍旧达到99%以上,具有优异的抗菌性及良好的耐洗涤性能。另外,植物还原法制备的纳米银溶液整理后的棉织物紫外线防护系数(UPF)值达到了36.82,具有较好的抗紫外性能。     

纳米氧化锌和纳米银对棉织物的多功能整理

以植物金银花提取物作为还原剂制备了纳米ZnO和纳米Ag,通过浸轧法将纳米ZnO单独整理以及将两者依次整理到棉织物上制备多功能棉织物(ZnO-棉织物、ZnO/Ag-棉织物).利用SEM、XRD、FTIR分析了整理前后棉织物的形貌和结构,并探讨了整理后棉织物的多功能性.结果表明,棉织物上的纳米粒子分布较均匀且发生了轻微团聚.与ZnO-棉织物相比,ZnO/Ag-棉织物对亚甲基蓝(MB)和红酒的降解率分别提高了7.09％和10.61％,说明纳米Ag提升了纳米ZnO的光催化活性.ZnO-棉织物经过10次洗涤后其纳米粒子含量虽有小幅下降,但对MB的降解率仍达到83.24％以上,说明负载纳米粒子后棉织物具有良好的自清洁能力和耐洗性能.此外,ZnO-棉织物和ZnO/Ag-棉织物的紫外防护系数(UPF)值分别达到33.23和41.06,对大肠杆菌和金黄色葡萄球菌的抑菌率均达到95％以上,表现出优良的抗紫外线性和抗菌性能.     

Effect of in situ deposition of calcium carbonate in cotton fiber on its mechanical properties

In this study, in order to improve mechanical properties of cotton fabrics, nano-micro sized calcium carbonate (CaCO₃) was deposited in situ on cotton fabrics. The mechanical properties, surface morphology, crystalline index, infrared spectrum, thermal property, and wettability of the deposited fabrics were measured and discussed. The results showed that the breaking strength of cotton fabric increased by about 10% after in situ deposition of nano-micro calcium carbonate. After ultrasonic washing, the strength of cotton fabric deposited CaCO₃ was still increased by about 10%. The crystallinity of the cotton fabric deposited with calcium carbonate increased from 76% to 84%. The hydrogen bond between cellulose molecules and calcium carbonate was confirmed by infrared spectroscopy. The hydrophilicity and thermal properties of cotton fabric were not significantly influenced by calcium carbonate deposition. This provides a new idea for improving the mechanical properties of cotton fabric.