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Artificial silk

Artificial silk, also known as or viscose, is a semi-synthetic made by regenerating from natural sources such as wood pulp or linters. It was developed to mimic the appearance, luster, and feel of natural while being more affordable and versatile. Unlike fully synthetic fibers like or , retains some traits, including high absorbency (up to 13% moisture regain) and breathability, making it suitable for and textiles. Invented in the late amid silk shortages in , the fiber's production revolutionized textiles by the mid-20th century, when rayon comprised a significant share of global fiber output. Pioneered by French inventor Count Hilaire de Chardonnet, who patented a nitrocellulose process in 1884 and began production in 1891, early versions were flammable. The safer viscose process, developed by Charles Frederick Cross and Edward John Bevan in 1892, dominated thereafter and was first commercialized in 1905. The term "" was standardized in 1924 by the . Today, rayon variants like and offer enhanced and , with global valued at approximately $20 billion as of 2024 and growing due to eco-friendly innovations. Widely used in apparel, home goods, and industrial applications, its raises environmental concerns from chemical use, though modern methods mitigate impacts. Detailed , processes, , and uses are covered in subsequent sections.

Definition and Overview

Definition

Artificial silk refers to a category of man-made fibers, specifically regenerated fibers produced from natural polymers such as wood pulp or other plant-based sources, engineered to mimic the luster, drape, smoothness, and overall tactile qualities of natural . These fibers are created by dissolving purified and extruding it through spinnerets to form filaments, resulting in a versatile material that combines the renewability of natural origins with industrial scalability. Unlike fully synthetic fibers, artificial silk is semi-synthetic in nature, as it derives from naturally occurring but undergoes chemical processing to achieve its fibrous form, making it an early example of bio-based innovation in . Developed in the late , it emerged as an affordable alternative to scarce and expensive natural , enabling broader access to silk-like garments and fabrics during a period of growing textile demand. The term "artificial silk" originated in the to market the pioneering products of French inventor Hilaire de Chardonnet, whose nitrocellulose-based fibers—later refined into modern —were the first commercially viable man-made silk substitutes, distinguishing them from sericulture-derived while highlighting their imitative properties. This nomenclature underscored the material's intent to replicate 's aesthetic and functional appeal without relying on silkworm production.

Distinction from Natural and Synthetic Fibers

Artificial silk, commonly referred to as , occupies a unique category in textile fibers as a regenerated material, distinct from both natural and fully synthetic options. Natural is a protein-based fiber, primarily composed of , secreted by the silkworm to form cocoons. This natural fiber exhibits a triangular cross-section with rounded corners, which refracts light to produce its signature luster and sheen. In comparison, artificial silk is derived from , a extracted from renewable plant sources like wood pulp or linters, which is chemically dissolved and extruded to form fibers. Lacking the and triangular cross-section of natural , artificial silk's appearance is engineered through processing to imitate the drape and gloss of genuine , though it absorbs moisture differently and may feel cooler against the skin. Unlike fully synthetic fibers, artificial silk is classified as semi-synthetic due to its base in natural rather than purely . Synthetic fibers such as and are polymerized from feedstocks, forming long-chain polyamides or polyesters through reactions like condensation polymerization. For instance, is produced from and , both derived from refining. This origin makes synthetics non-biodegradable and reliant on fossil fuels, whereas artificial silk's foundation allows for greater environmental renewability, though its production involves chemical solvents that require careful management. Consequently, artificial silk bridges the gap between the biodegradability of natural fibers and the engineered consistency of synthetics. Historically, artificial silk's development and naming reflected efforts to position it as an accessible alternative amid economic and regulatory pressures. In the early , it was promoted as a "silk substitute" to distinguish it from natural , enabling manufacturers to circumvent higher import duties and trade restrictions levied specifically on genuine silk products. This strategic differentiation allowed broader market access without competing directly under silk's protected status. However, the advent of true synthetics, such as invented in 1935 by DuPont researchers, eventually eclipsed artificial silk in sectors demanding higher strength and elasticity, shifting perceptions from a premium mimic to a versatile but secondary option.

History

Early Inventions

The earliest documented attempt to produce artificial silk dates to 1855, when chemist Georges Audemars secured British Patent No. 283 for a involving the of mulberry tree bark pulp in a viscous mixed with gummy substances to form fibers. Audemars achieved this by dipping a needle into the and drawing out threads, creating a crude that mimicked silk's appearance. However, the process proved highly impractical, yielding fibers that lacked sufficient strength and uniformity for practical use, thus remaining an experimental curiosity rather than a viable . A major advancement came in 1884 with French engineer and count Hilaire Bernigaud de Chardonnet, who patented the first commercially feasible artificial silk, known as "Chardonnet silk," based on derived from . His process began with treating or wood pulp to form , dissolving it in ether and alcohol to create , and extruding the viscous solution through fine glass capillaries or early spinnerets to produce continuous filaments that solidified in warm air. The filaments were then subjected to denitration using chemical treatments, such as ammonium sulfide, to remove groups and restore a more silk-like composition. This breakthrough was showcased to great acclaim at the 1889 Exposition, where samples of the shimmering, silk-resembling threads demonstrated its potential as an alternative to natural . Early artificial silk fibers, including Chardonnet's, encountered significant hurdles that curtailed their immediate success. The remnants made the material highly flammable, earning it the derogatory nickname "mother-in-law silk" among factory workers due to its dangerous ignition properties. Additionally, the fibers degraded rapidly, becoming brittle and discolored from chemical instability and exposure to environmental factors, which compromised their longevity and usability. These limitations—rooted in the inherent volatility of —restricted adoption until subsequent refinements addressed safety and durability concerns.

Commercial Development

The viscose for artificial silk was invented in 1891 by chemists Charles Frederick Cross, Edward John Bevan, and Clayton Beadle, who developed a method to dissolve using and , forming a xanthate solution that could be extruded and regenerated into fibers. They patented this in 1892, marking a pivotal advancement in producing silk-like filaments from abundant sources like wood pulp. Commercial production commenced in 1905 when the British firm established the world's first viscose rayon factory in , , enabling scalable of the fiber initially marketed as "artificial silk." In the United States, the American Viscose Company, a subsidiary, opened the first commercial plant in , in 1910, producing about 1.4 million pounds annually by 1911 and spurring rapid industry growth. Global expansion accelerated in , with viscose factories established in countries like by the early 1910s, alongside earlier rayon production using alternative processes such as cuprammonium since 1899. The economic impact was profound, as artificial silk reduced dependence on expensive natural silk imports from . By the , U.S. production surged from approximately 3 million pounds in 1919 to 123 million pounds in 1929, fostering a $100 million industry that employed thousands and diversified . further propelled , as silk shortages prompted increased rayon output for applications like bandages, conserving natural silk for critical military needs such as parachutes.

Production Process

Raw Materials

The primary raw material for artificial silk, particularly in the production of viscose rayon, is derived from natural sources such as wood pulp or linters. Wood pulp is typically sourced from trees like and , or hardwoods such as and , which provide high-quality fibers suitable for regeneration. linters, the short fibers adhering to seeds after ginning, serve as an alternative source, offering a purer form of with minimal impurities. These materials are selected for their high content, typically around 40-50% in raw form, which is essential for efficient processing into fibers. Global demand for specifically used in production has been significant, with viscose staple output relying on approximately 5.8 million tonnes of annually as of 2021, reflecting the scale of the industry in the . This demand underscores the reliance on sustainable practices and agricultural byproducts to meet production needs without depleting resources excessively. Preparation of the begins with pulping the raw materials to isolate the fibers, followed by purification to achieve a high alpha- content of at least 95%, which ensures and quality in the final . This purification involves bleaching with chlorine-based or oxygen-based agents to remove , the binding component in wood that imparts color and rigidity, and —often through acid or enzymatic treatment—to break down and eliminate , a that hinders dissolution. The resulting is highly refined, with minimal residual carbohydrates, making it ideal for chemical conversion. In addition to cellulose, the production process requires several auxiliary chemicals to facilitate the transformation. (NaOH) is used for alkalization, swelling the cellulose sheets to prepare them for further reaction. (CS₂) is essential for the xanthation step in the viscose process, where it reacts with the alkali cellulose to form a soluble compound, though its high toxicity poses health risks to workers, including neurological and cardiovascular effects from prolonged exposure. Sulfuric acid (H₂SO₄) forms part of the spinning bath, where it coagulates the viscose solution into fibers during extrusion. These reagents are handled under strict controls due to their corrosive and hazardous nature.

Manufacturing Steps

The manufacturing of artificial silk, primarily through the viscose process, transforms purified into a viscous suitable for into fibers via a sequence of chemical treatments and mechanical operations. This method, which regenerates cellulose in form, relies on controlled reactions to achieve the desired properties. The process assumes high-purity cellulose input, typically from wood pulp, and emphasizes precise control over concentrations, temperatures, and durations to ensure solution stability and fiber quality. The initial step involves cellulose sheets in an aqueous solution to form alkali cellulose. The sheets are immersed in approximately 18% NaOH at around 45°C for about 20 minutes, with continuous stirring to facilitate swelling and reaction. Following steeping, the mixture is pressed to remove excess liquor, yielding alkali cellulose with 30-35% solids content by adjusting the press to 2.5-3.0 times the original pulp weight. The pressed alkali cellulose is then shredded into small crumbs to increase surface area for subsequent reactions. These crumbs are aged for 24-72 hours at controlled temperatures, typically around 23°C, allowing oxidative that reduces the molecular weight by 2-3 times and develops the appropriate for further processing. Next, the aged crumbs undergo xanthation by reaction with (CS₂) in a closed vessel for about 2.5-3 hours at 30-35°C, forming sodium xanthate, a soluble compound. This xanthate is then dissolved in a dilute NaOH (around 5-8%) with agitation for 3 hours at low temperature (e.g., 5°C), producing a viscose spinning containing 8-10% . The core reactions in viscose formation are as follows: \text{Cellulose} + \text{NaOH} \rightarrow \text{Alkali cellulose} \text{Alkali cellulose} + \text{CS}_2 \rightarrow \text{Cellulose xanthate} These steps yield a stable xanthate derivative that enables dissolution. Finally, the ripened viscose solution is extruded through fine holes in a spinneret into a coagulating bath of sulfuric acid (typically 10-15% H₂SO₄), sodium sulfate, and zinc sulfate at 40-50°C, where the cellulose regenerates as continuous filaments through acid-induced decomposition of the xanthate. The emerging filaments are drawn to orient the structure, washed to remove residual chemicals, and dried to produce the finished artificial silk fibers.

Types

Viscose Rayon

Viscose rayon is a regenerated produced through the viscose process, in which purified from wood pulp or other natural sources is chemically dissolved and extruded to form continuous or staple fibers. This semi-synthetic material mimics the qualities of , offering a soft, smooth and high absorbency due to its cellulosic . It is commonly produced in form for woven fabrics or as staple fibers for spinning into yarns, with individual fiber typically ranging from 1 to 5 denier to achieve a silk-like fineness and drape. The viscose process was patented in 1892 by British chemists Charles Frederick Cross and Edward John Bevan, marking the foundation of commercial artificial silk production. This innovation rapidly gained prominence, dominating the market for regenerated fibers until the 1950s, when the rise of fully synthetic alternatives like began to shift industry preferences. Viscose rayon's distinctive luster, which contributes to its silk-like appearance, results from the extrusion process; however, delustering agents such as can be incorporated into the spinning solution to produce a finish, reducing reflectivity while maintaining other properties. Key to viscose rayon's is the aging step, where alkali cellulose sheets are stored under controlled temperature and humidity to depolymerize the chains, thereby regulating molecular weight and achieving the desired solution , typically 30-50 poise for standard textile-grade . This step ensures the viscose dope flows appropriately during wet spinning, where it is extruded into an acid bath to regenerate the . Global of viscose reached approximately 6 million tonnes annually as of 2023, with over 70% concentrated in —primarily and —driven by demand in apparel and textiles.

Cellulose Acetate and Other Variants

Cellulose acetate rayon, a derivative of , is produced by first acetylating purified —typically sourced from wood pulp or linters—with in the presence of acetic acid and a catalyst to form flakes. These flakes are then dissolved in acetone to create a spinning solution, which is extruded through spinnerets and dry-spun in warm air to form continuous filaments that solidify upon of the . This process, invented in 1904 by brothers and Dreyfus through their experiments on partially hydrolyzed soluble in acetone, marked a significant advancement in semi-synthetic s. Commercial production began in the , with British Celanese starting fiber manufacturing in 1921 and the first U.S. acetate produced by the in 1924. Unlike regenerated fibers, exhibits properties and lower flammability, making it suitable for applications requiring heat-settable and less ignitable materials. A primary non-textile use is in filters, where its porous structure effectively traps and while comprising over 95% of global filter production due to its efficiency and durability. Global production of , including fibers, stands at approximately 850 kilotons annually as of , reflecting its established role in both textiles and . Cuprammonium rayon, another cellulose-based variant, involves dissolving cellulose in Schweizer's reagent—a complex of copper(II) hydroxide and ammonia—to form a viscous solution that is wet-spun through spinnerets into a coagulating bath of dilute sulfuric acid, regenerating the cellulose fibers while precipitating copper compounds. This process originated in the 1890s in Germany, where chemist Eduard Schweizer's 1857 discovery of cellulose solubility in cuprammonium solutions was commercialized through patents by Joseph Pauly in 1897, leading to factories by Glanzstoff-Fabriken in 1899. The method enables production of exceptionally fine filaments, down to 0.5 denier, yielding fibers with silk-like softness, subdued luster, and superior drapability for lightweight apparel. However, the process generates copper-laden wastewater, posing environmental challenges due to heavy metal effluent that requires treatment to mitigate aquatic toxicity. Among other variants, represents an eco-friendlier evolution, where is directly dissolved in N-oxide (NMMO) solvent and dry-jet wet-spun to regenerate fibers in a closed-loop system that recovers over 99% of the solvent, reducing chemical waste compared to traditional methods. Introduced commercially in the by Fibres as Tencel, with initial production at a plant in 1990 and expansion in , by 1998, offers enhanced tensile strength and breathability for sustainable textiles. , a high-tenacity modification of viscose , achieves greater wet strength through treatment of before xanthation, resulting in fibers with improved durability and modulus for stretch-resistant fabrics. Developed initially in and refined in by the , is derived from beech pulp and used in intimate apparel for its softness and shape retention.

Properties

Physical Characteristics

Artificial silk, primarily referring to regenerated cellulose fibers such as viscose rayon, exhibits tensile strength ranging from 1.5 to 2.4 grams per denier in the dry state, though this value decreases to 0.7 to 1.2 grams per denier when wet due to fiber swelling and water absorption. at break typically measures 15 to 25 percent under dry conditions, providing moderate flexibility comparable to natural 's 20 to 25 percent but with less overall resilience. In contrast to natural , which maintains higher dry tensile strength of 3.5 to 5.1 grams per denier, artificial silk's mechanical properties make it suitable for lightweight applications but more prone to weakening during laundering. The appearance of artificial silk fibers is characterized by high luster, derived from their multilobal or serrated cross-section that reflects light, though differing from silk's structure, resulting in a silky sheen often enhanced during . Texture-wise, these fibers have a regain of 11 to 13 percent at standard conditions (65 percent relative humidity and 21°C), which contributes to excellent drape and but also leads to wrinkling and reduced dimensional in humid environments. This affinity exceeds that of many synthetics but aligns closely with silk's 10 to 11 percent regain, enhancing comfort in apparel while requiring careful handling to avoid creasing. Density for artificial silk fibers averages 1.5 grams per cubic centimeter, slightly higher than natural silk's 1.3 to 1.4 grams per cubic centimeter, influencing their weight and packing in fabrics. Thermally, viscose variants decompose at 180 to 200°C without melting, while cellulose acetate types soften around 180 to 200°C and fully melt near 230°C, differing from natural silk's decomposition above 250°C and providing distinct processing limitations for heat-sensitive uses.

Chemical Properties

Artificial silk, primarily composed of regenerated cellulose such as viscose rayon and , exhibits limited chemical stability due to its polar hydroxyl groups, making it more vulnerable to degradation than fully synthetic fibers like or , which have stronger hydrophobic structures. Viscose rayon dissolves in cold concentrated , such as 60% w/w solutions, and is disintegrated by hot dilute or cold concentrated mineral acids like HCl, though it remains stable in dilute acids for short exposures but weakens significantly with prolonged contact. Strong alkali solutions, particularly those above 10, cause swelling and substantial loss in strength, rendering the fiber unsuitable for harsh basic environments without protective treatments. In terms of flammability, viscose rayon burns readily similar to , with a limiting oxygen index (LOI) of 17-19%, igniting easily in air and producing a steady flame, whereas natural chars rather than sustains burning due to its higher LOI of 22-23%. Cellulose variants, while also flammable, often melt during , which can lead to self-extinguishing behavior in certain configurations by reducing oxygen access to the fabric core. Degradation of artificial silk occurs primarily through under combined heat and moisture, leading to significant tensile strength loss under prolonged to high and , far exceeding the stability of synthetics that retain over 80% strength in similar exposures. UV further accelerates by breaking chains, reducing strength by 20-30% without stabilizers, highlighting the need for additives in outdoor applications.

Applications

Textile Uses

Artificial silk, commonly known as , plays a central role in apparel production, where it is valued for its silk-like sheen and that mimic natural fibers while offering affordability. Approximately 33% of rayon fibers are directed toward apparel applications as of 2024, supporting a range of garments that prioritize comfort and aesthetic appeal. In , is frequently employed for dresses, blouses, and linings, providing a soft, drapable ideal for everyday and . Viscose crepe de chine, a lightweight variant, is particularly favored for its subtle crinkle and fluid movement in items like blouses, summer dresses, and scarves, enhancing their elegant yet breathable qualities. Its moisture-absorbing properties contribute to a natural drape that allows garments to flow gracefully without clinging. For home textiles, rayon is incorporated into curtains, , and , where its softness and ability to regulate temperature promote everyday comfort and durability. Blends with , such as 50/50 combinations, enhance wrinkle resistance while retaining , making these fabrics practical for items like bedsheets and draperies that withstand frequent use. Historically, rayon's introduction as "artificial silk" in the revolutionized fashion by enabling the popularization of dresses, which embodied the era's liberated style as an accessible luxury alternative to expensive natural . In contemporary applications, advanced rayon variants like are integrated into activewear, leveraging their stretch and moisture-wicking attributes for performance-oriented clothing such as and .

Industrial and Other Uses

Artificial silk, particularly high-tenacity , serves as a in applications requiring strength and under . In the automotive sector, it is widely used for tire cords in heavy-duty s, such as those for , motorcycles, and off-road , where its high tensile strength and heat resistance help maintain structural integrity during extreme conditions. Similarly, high-tenacity rayon yarns reinforce conveyor belts and hoses, providing flexibility and resistance to abrasion in and environments. Its fine structure also makes rayon suitable for media in air and systems, where it forms porous cartridges that effectively trap , oils, and chemicals while allowing fluid passage. In medical applications, rayon-based materials are valued for their absorbency and . Non-woven rayon pads are commonly used in surgical dressings and bandages, offering high fluid absorption to manage while featuring a non-adherent surface that minimizes to during changes. Cellulose acetate, another variant of artificial silk, dominates the production of cigarette filters, utilizing its porous tow structure to reduce and inhalation; it is incorporated into the vast majority of the estimated 5.7 trillion s smoked annually worldwide as of 2022. Beyond these sectors, artificial silk finds utility in packaging and historical military contexts. Regenerated cellulose, known as , serves as edible or peelable casings for food products like sausages, providing a transparent, breathable barrier that maintains product freshness and shape during processing. fibers are also applied in paper coatings to enhance surface smoothness and printability in specialty . During , emerged as a critical substitute for in parachute production amid global shortages, enabling large-scale manufacturing to support airborne operations across Allied forces.

Environmental Impact

Production Effects

The production of artificial silk, particularly viscose rayon, is highly resource-intensive, requiring substantial and inputs. Blue water consumption, which accounts for direct freshwater use in processing, typically ranges from 80 to 370 liters per kilogram of fiber, depending on the such as batch or continuous washing. Energy demands are also significant, with pulping processes consuming approximately 12 per kilogram on average, driven by generation, drying, and chemical reactions in the viscose process. These inputs contribute to broader environmental strain, as production sites are often located in water-scarce regions, exacerbating local . Chemical pollution from viscose manufacturing poses severe risks due to the release of toxic substances like (CS₂), a neurotoxic agent used in the xanthation step. Emissions of CS₂ vary by product type, averaging around 100 kg per ton for viscose staple fiber and up to 284 kg per ton for viscose , leading to atmospheric and . (H₂S) accompanies these releases at 20-33 kg per ton, and together, CS₂ and H₂S account for 10-20% of air pollutants from plants, contributing to and respiratory hazards in surrounding communities. CS₂'s volatility results in fugitive emissions during handling and recovery, with U.S. facilities reporting thousands of pounds discharged annually to air and water despite treatment efforts. Sourcing raw from wood plantations drives , with an estimated 300 million trees logged annually for global viscose production as of 2024, leading to habitat loss in biodiversity hotspots. In regions like , pulp concessions supplying viscose have resulted in over 170,000 hectares of natural forest loss between 2015 and 2019 due to clearing and fires. This , often exceeding 100,000 hectares per year in high-production areas, releases stored carbon and disrupts ecosystems. Worker is further compromised by CS₂ , causing "viscose rayon ," a condition involving , cardiovascular abnormalities, and neurotoxic effects such as parkinsonism-like symptoms from chronic inhalation. Studies of workers show elevated risks of coronary heart disease and damage at levels above 10 , with historical cases linking high CS₂ concentrations to irreversible impairments.

Sustainability and Alternatives

Efforts to enhance the sustainability of artificial silk production focus on implementing closed-loop systems that recover and reuse chemicals, minimizing waste and emissions. For instance, Lenzing Group's production of fibers employs a closed-loop process that recovers over 99% of the N-oxide (NMMO) solvent, a non-toxic alternative to the used in traditional viscose manufacturing. This approach significantly reduces chemical discharge into the environment compared to conventional viscose processes, which often rely on open-loop systems with lower recovery rates. In viscose production, companies like Lenzing are advancing closed-loop technologies for key chemicals such as (CS₂) and compounds, achieving recovery rates of up to 95% for sulfur in member facilities of the Commonwealth Viscose (CV) initiative. The process, in particular, further contributes to by using solvents that enable near-complete , thereby lowering overall emissions and resource consumption relative to viscose. As of 2024, the Canopy Hot Button Report indicates that 53% of the global supply of viscose, , , and other man-made cellulosic fibers comes from producers rated green or higher for practices. Regulatory measures play a crucial role in mitigating health and environmental risks associated with artificial silk production. The Union's REACH regulation classifies CS₂ as a due to its toxicity, with an indicative value of 10 mg/m³ as an 8-hour time-weighted average to protect workers from neurotoxic effects. Additionally, certifications such as Standard 100 verify that rayon and viscose textiles meet stringent criteria for harmful substance content, ensuring low-impact production and safe end products for consumers. These standards encourage manufacturers to adopt cleaner processes and traceable supply chains. Emerging alternatives to traditional artificial silk emphasize bio-based and recycled materials that offer similar aesthetic and functional properties with reduced environmental burdens. fibers, derived from , serve as a biodegradable option for textiles mimicking silk's drape and softness, with applications in apparel and nonwovens due to their renewability and lower during production. Recycled variants engineered to replicate silk's sheen and provide another synthetic mimic, utilizing to decrease reliance on virgin petroleum-based resources. There is also a growing shift toward natural and semi-natural fibers, such as ethically sourced silk or bamboo-derived and , which offer comparable breathability and luster while avoiding the chemical-intensive steps of production. The market for sustainable cellulosic fibers, including eco-friendly variants, has expanded notably since 2010, driven by consumer demand and supported by a of around 8% for the broader sector through the 2020s.

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