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Chitosan-Based Sustainable Textile Technology: Process, Mechanism, Innovation & Safety


         precipitated on the fabric surface.  are controlled by the ratio of chitosan  to fabrics for improving durability,
                                            and CF3(CF2)7SO3Li concentrations.  desirable aroma, hygienic use, fire
         The SEM study confirms that        For the treatment of fabric, the   resistance, wound healing activity, and
         nanofiberlike shapes are deposited on  nanoparticles dispersion sprayed over  so on. A tiny amount of active
         the fiber surface, resulting in rough  the textile surface. The contact angle  components is surrounded by a
         surface on microscale cotton fiber  of the treated fabric is 157° ± 2.2°.  continuous polymeric phase in the
         structure. Also, nanoflower-like                                      microencapsulation process. The
         precipitation is found for the same  It has been noticed that long-term  active component is introduced in
         treatment with polyester fabrics. The  water contact would degrade the  different terms such as core, internal
         deposition of chitosan nanosized   particles due to the presence of   phase, encapsulated, while the
         particles forms proper roughness on  hydroxyl groups in the chitosan  continuous polymeric phase is
         cotton and polyester fibers. Besides,  complex. The  hydroxyl  groups  are  described as coating, wall, shell,
         an emulsion of polysiloxane may be  blocked by treating the fabric with  external phase, and membrane. The
         used for reducing the surface energy  chlorodimethyl-1H-1H-2H-2H-     continuous polymeric phase is one of
         of the chitosan-treated fabric.    perfluorodecylsilane (90%) in 1%   the vital issues for application-based
                                            heptane solution. The contact angle  microencapsulation process. Chitosan
         The emulsion is prepared by        has been improved after this treatment  is very efficient to encapsulate the
         hexadecyltrimethoxy silane (HDTMS,  and found at 160° ± 2° [78].      core materials in microencapsulation
         85%), 3-glycidol-propyl-trimethoxy-                                   process. The core materials are usually
         silane (GPTMS, 97%), and sodium    Chitosan: a coating on textile for UV  found in two different phases-solid and
         dodecyl sulfate (SDS). A mixture of 8g  blocking                      liquid-and chosen for specific
         HDTMS, 2g GPTMS, and 1g SDS is                                        application. The grapefruit seed oil, a
         stirred at 75°C for 2 h maintaining pH  A coating of chitosan-graphene is  liquid core material, is used to attain
         about 2 using HCl. The operation   designed for the process of developing  durable fragrance and antibacterial
         temperature is reduced to room     a cotton fabric as UV blocker.  A  properties by microencapsulation
         temperature, and the pH is maintained  graphene nanosheet (1–3 nm) is added  process in the textile application [81].
         at 8.0 by ammonia. After the dipping,  to chitosan solution by stirring  Chitosan is one of the shell materials
         padding, washing, and drying, the  vigorously around 5 h. A cotton fabric  which are used for microencapsulation
         curing process is done at 150°C for 1  is submerged in the dispersion of  due to nontoxic, biodegradable, and
         min. Further washing is necessary if  chitosan-graphene for 2 h. In padding  naturally extracted. Depending on the
         excess SDS is present on the fabric  process, the fabric passes through two  process, different types of solvents,
         surface and need to cure again     dips and two nips for achieving 80%  crosslinking agents, and surfactants
         following the same process. In     wet pick up on average. The washing  could be used to modify the mechanical
         characterization, water contact angles  and drying treatments are maintained  strength of chitosan shell for releasing
         (WCA) are found 152° and 148° for  separately. The predrying process is  active core materials.
         cotton and polyester, respectively. The  continued at 70°C for 10 min and curing
         cotton and polyester fabrics having  process at 110°C for 10 min. The  Microencapsulation processes
         WCA at 130° and 102°, respectively,  ultraviolet protection factor (UPF) of the
         after processing only with chitosan do  treated fabric using 1% graphene is 60  There  are  many  different
         not exhibit long duration hydrophobicity.  times greater than that of untreated  microencapsulation techniques such
                                            cotton. The well-dispersed graphene  as coacervation [82], interfacial
         Another process based on fluorocarbon  particle in the chitosan matrix without  polymerization  or  in  situ
         to reduce the surface energy has been  any aggregation is considered for the  polymerization, air suspension coating,
         developed for the preparation of   high value of UPF [80].            emulsion hardening process, pan
         superhydrophobic textile. In this                                     coating, spray drying [83, 84],
         process, anionic heptadecafluoro-1-  Chitosan microcapsules for textile  centrifugal extraction [85], etc. (Figure
         octanesulfonate has been synthesized  applications                    7).
         from a surfactant, CF3(CF2)7SO3Li.
         Chitosan nanoparticles are formed  The microencapsulation technique is  The simple coacervation technique is
         using 0.2% chitosan solution and   widely used in pharmaceutical,     usually followed by single colloidal
         mixed with soluble heptadecafluoro-1-  cosmetic, food, biotechnology, textile  solute while complex coacervation
         octanesulfonate in acetic acid. The  industries to obtain control release of  process involving more than one
         dispersion is stirred for 1 h and left it  active components for a particular  colloidal solute. The coacervation is
         for 2 h before characterization. The size  purpose.  In  general,  the  one of the mostly used techniques for
         and surface charge of the chitosan NPs  microencapsulation process is applied  the development of smart textile and


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