Polyethylene Terephthalate Research Articles

More Efficient Chemical Recycling of Poly(Ethylene Terephthalate) by Intercepting Intermediates.

The research presented in this paper offers insight into the availability of intermediates in the depolymerization of polyethylene terephthalate (PET) to be used as feedstock to create value-added products. Monitoring the dispersity, molecular weight, end groups, and crystallinity of reaction intermediates during the heterogeneous depolymerization of PET offers insight into the mechanism by which the polymer chains evolve during the reaction. Our results show dispersity decreases and crystallinity increases while the yield of insoluble PET remains high early in the reaction. Our interpretation of this data depicts a mechanism where chain scission targets amorphous tie chains between crystalline phases. Targeting the tie-chains lowers the Mn of the polymer without changing the amount of recovered polymer flake. Chain scission of tie-chains and isolating highly crystalline PET lowers the dispersity (Đ) of the polymer chains, as the size of the crystalline lamellae guides the molecular weight of the depolymerized oligomers. When sufficient end groups of PET chains are converted to alcohol groups, the PET flakes break apart into highly crystalline and less disperse polymer. Our results also demonstrate that the oligomeric depolymerization intermediates are readily repolymerized, offering new opportunities to chemically recycle PET more effectively and efficiently, from both an energy and purification standpoint.

Alloplastic Vascular Grafts for Venous Interposition in Pancreatic Surgery: Readily Available and Reliable.

To investigate patency and clinical outcomes of alloplastic and other venous interposition graft materials in pancreatic surgery. Vascular pancreatic surgery is increasingly performed for locally advanced pancreatic neoplasms. Different than other centers, we prefer to use alloplastic vascular graft materials for superior mesenteric vein and portal vein interposition in pancreatic surgery. Advantages are off-the-shelf availability at any customizable length, different diameters, and ring-enforcement but proposed concerns are their thrombogenicity and fatal complications. Patients who underwent elective pancreatic resections with mesoportal venous interposition grafts (ISGPS type 4) between 2003-2022 were identified from the institutional pancreatectomy registry. Alloplastic vascular grafts imply synthetic materials, either based on polytetrafluorethylene (PTFE) or polyethylene terephthalate (PET). Surgical details, clinicopathological, and follow-up data were analyzed. The patients were followed for graft patency by cross-sectional imaging. In this study, 201 patients with venous interposition grafts were included (23% simultaneous arterial resections). Total pancreatectomy (41%) and pancreatoduodenectomy (35%) were the most frequent procedures. Vascular graft materials were alloplastic in 180 patients (83% PTFE and 17% PET) with a median diameter of 10mm and a median length of 33mm (measurement by CT scan). Patency rates among all graft materials at 7-, 30-, and 90-days were 99%, 93%, and 87%. Alloplastic grafts demonstrated superior patency over other materials (hazard ratio 2.7, P=0.009), and PTFE reached a 1-year patency of 78%. The all-cause 90-day mortality rate was 10%. No graft infection occurred. Alloplastic venous vascular grafts are safe and readily available tools in pancreatic surgery, especially for long-segmental mesoportal venous reconstructions.

Selective Degradation of Polyethylene Terephthalate Plastic Waste Using Iron Salt Photocatalysts.

Plastic pollution poses a significant challenge to environmental conservation. Efficient recycling of plastic is a key strategy to address this issue. Polyethylene terephthalate (PET), commonly found in plastic bottles, represents a substantial portion of plastic waste. Consequently, the efficient degradation and recycling of PET is crucial for the sustainable development of society. However, the implementation of methods for PET depolymerization and recycling typically necessitates alkaline/acidic pre-treatment and significant energy input for heating. Here, we propose a gentle, and highly efficient photocatalysis approach for selectively degrading PET plastic waste into terephthalic acid (TPA) in high yield (up to 99%) using cost-effective iron salts. Notably, this method achieved excellent selectivity with high TON and TOF values, applying oxygen or air as environmentally friendly oxidants. In addition, the solvent can be recycled without compromising the TPA yield, and large-scale reactions can be performed smoothly.

Comprehensive and Robust Anti-Jamming Dual-Electrode Pair Sensor.

Capacitive flexible sensors often encounter instability caused by temperature fluctuations, electromagnetic interference, stray capacitance effects, and signal noise induced by ubiquitous vibrations. The challenge lies in achieving comprehensive anti-jamming abilities while preserving a simplistic structure and manufacturing process. To tackle this dilemma, a straightforward and effective design is utilized to achieve comprehensive and robust anti-jamming properties in capacitive sensors. Electrospinning thermoplastic polyurethane (TPU) fiber mats soak with ionic liquid (IL) to create a co-continuous structure (TPU@IL) with high ionic conductivity and dielectric constant, which acts as the sensing units. The sensing mechanism of the TPU@IL with multiple electrode pairs encapsulated by polyethylene terephthalate (PET) is systematically elucidated. The optimal dual-electrode pair design for capacitive and resistive sensors, which have different sensitivities to temperature and stress, simultaneous realizes temperature-stress dual-mode sensing. Remarkably, the sensitivity curve of the TPU@IL/PET capacitive sensor exhibits an intriguing rarely reported S-shape with an adjustable step stress point. No liquid leakage even during extensive stress-strain cycling (>4000 cycles). Despite a slight compromise in sensitivity and response time, the TPU@IL/PET sensor demonstrates exceptional electromechanical stability, reliability, and powerful anti-jamming abilities against various interferences. A simple yet innovative sensor design enhances the performance and applicability of capacitive sensors in challenging environments.

Durability of non-woven geotextiles produced from recycled polyethylene terephthalate (PET)

Achieving the goals of sustainable development and circular economy requires recycling and reusing plastic materials. In this research, the durability of five needle-punched non-woven geotextiles were experimentally studied. The geotextiles were made of recycled PET (rPET), virgin PET (vPET), and combinations of rPET and vPET fibers. The samples were hydrolyzed for a period of 14, 28, and 56 days and the retained tensile strength and puncture resistance of the samples were determined at the end of each interval. Moreover, this study took the benefits from the capability of differential scanning calorimetry (DSC), Fourier transforms in infrared spectroscopy (FTIR) analysis, and scanning electron microscopy (SEM) images to interpret the results acquired. Testing on as-received products, it was understood that recycling process could increase crystallinity of the fibers, increasing the fibers fragility, reducing the tensile strength and elongation capacity of rPET fibers. Moreover, considering the borderline value of 50% retained strength, a shorter service life (up to 30%) of rPET products in comparison with vPET products, due to higher degradation rates, was observed.

A flexible plasmonic substrate for sensitive surface-enhanced Raman scattering-based detection of fentanyl.

In this work, we demonstrate a straightforward and versatile approach for fabricating flexible SERS substrates for highly sensitive fentanyl detection. Our design strategy integrates the synthesis of a yolk-shell structured plasmonic nanomaterial with a flexible cellulose substrate. The resulting SERS platform demonstrates excellent sensing capabilities, achieving a fentanyl detection limit as low as 4.89 ng mL-1.

A Double‐Arch‐Structured Hybrid Triboelectric and Piezoelectric Nanogenerator Based on Polyvinylidene Fluoride/Graphene Oxide Composite Films

In this study, a methodology for fabricating double‐arch triboelectric and piezoelectric composite nanogenerators using polyvinylidene fluoride (PVDF) and graphene oxide (GO) is presented. Initially, nanofiber films comprising PVDF/GO are synthesized through electrostatic spinning. Subsequently, the PVDF/GO film is integrated with cotton fibers and a copper electrode to construct the triboelectric layer. In contrast, another portion of the PVDF/GO film, alongside a copper electrode, comprises the piezoelectric layer, with the central copper electrode acting as a common electrode. Finally, a double‐arch structure is established by employing polyethylene terephthalate film to facilitate synergistic operation between the triboelectric and piezoelectric layers. In the experimental results, it is indicated that the maximum open‐circuit voltage and short‐circuit current of the triboelectric layer of the double‐arch structure are 330 V and 36 μA, respectively, representing increases of 44% and 50% compared to those of the sandwich triboelectric structure. Additionally, the maximum open‐circuit voltage and short‐circuit current of the piezoelectric layer are 22 V and 4 μA, respectively, reflecting enhancements of 57% and 100% over those of conventional sandwich piezoelectric structures. The output power of the double‐arch composite nanogenerator is capable of lighting up 120 light‐emitting diodes. Thus, this composite nanogenerator shows great potential as an environmentally friendly energy source.

Task-Specific Deep Eutectic Solvent for Efficient Dissolution and Further Accelerating Alkaline Hydrolysis of Polyesters Into Their Monomers.

Polyester plastics have brought great convenience to modern society. However, the continuous accumulation of their production increasingly threatens human health. Polyethylene terephthalate (PET) is one of the largest type of polyester plastics and its recycling is a major challenge. In this work, deep eutectic solvent (DES) composed of thenyl alcohol and choline chloride (ChCl) was designed for efficient dissolution of PET at 165 °C for 20 min, and further accelerating complete alkaline hydrolysis of PET into its monomer terephthalic acid (TPA) and ethylene glycol (EG) with a high TPA monomer yield (98.2 %) in 25 min at 100 °C. Moreover, the designed DES is also efficient for dissolution and alkaline hydrolysis of other polyester plastics, including poly(trimethylene terephthalate) (PTT) and poly(ethylene furanoate) (PEF) into their monomers. This work provides a feasible and sustainable solution for the recycling of polyester wastes.

Crack Development and Electrical Degradation in Chromium Thin Films Under Tensile Stress on PET Substrates

The mechanical and electrical deterioration of chromium (Cr) thin films sputtered onto polyethylene terephthalate (PET) substrates under tensile strain was studied. Understanding mechanical and electrical stability due to imposed strain is particularly important for device reliability, as the demand for flexible electronic devices increases. Cr thin films, widely spread across the field of electronic and sensor applications, face crack propagation with electrical degradation with tensile stress that can seriously compromise the performance. Accordingly, this study offers new findings on how Cr film thickness might influence crack formation and electrical resistance differently and also the general guidelines for flexible electronic component design with respect to long-term durability. Electrical resistances were measured while mechanically stretching 100- and 200 nm thin sheets. The study focused on crack development and propagation mechanisms in both film thicknesses and their effects on percentage change in electrical resistance (PCER). Scanning electronic microscopy (SEM) was used to characterize surface morphology and observe cracks as the strain rose. Early crack formation in 100 nm Cr films led to rapid PCER increases due to quick crack propagation and fast electrical degradation. Thicker 200 nm films, however, showed a more gradual PCER rise with fewer but deeper cracks, indicating a regulated strain response. Unlike the sharp PCER spike in 100 nm films, 200 nm samples were more variable, with three out of four showing a slight PCER decrease at the end, hinting at partial crack repair or conductive realignment before full failure. These results underscore the role of layer thickness in managing crack propagation and electrical stability, relevant for flexible electronics and strain sensors. This paper is aligned with the ninth goal of the United Nations Sustainable Development Goals, specifically Target 9.5: Enhance Research and Upgrade Industrial Technologies.

Selective Oxidation of Polyesters via PdCu-TiO2 Photocatalysts in Flow.

Catalytic upcycling of plastic wastes offers a sustainable circular economy. Selective conversion of the most widely used polyester, polyethylene terephthalate (PET), under ambient conditions is practically attractive because of low energy consumption and carbon footprint. Here, we report selective, aerobic conversion of PET in a flow reactor using TiO2 photocatalyst modified with atomic Pd and metallic PdCu (Pd1Cu0.4-TiO2) under ambient conditions. We demonstrate that atomically synergistic Pd1Cu0.4-TiO2 exhibits a formate evolution of 4707 μmol g-1 h-1 with a selectivity of 92.3% together with trace COx released. Importantly, we show that this corresponds to 10-103 times greater activity than reported photocatalytic systems. We confirm that synergy between atomic Pd and metallic PdCu boosts directional charge transfer and oxygen-induced C-C cleavage and inhibits product decomposition. We conclude that photocatalytic waste plastic-to-chemical conversion is sustainable via targeted engineering of atomically synergistic catalysts and reaction systems.

Stabilizer Effects on the Gelation of Modified Recycled PET for 3D Printing Filament Application

This research identification gel types of the modified-recycled poly (ethylene terephthalate) (modified-rPET) filament, with and without the addition of heat stabilizer Pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate (Irganox®1010). This research also identifies the gel types and studies thermal behavior of the modified-rPET filaments above, by using a hot-stage microscopy, and a differential scanning calorimetry, respectively. rPET flakes were dried to deplete the moisture. Then, they were mixed with additives and heat stabilizer (Irganox®1010) at 0 and 0.5 pph, Then, they were extruded to be compound using twin screw extruder. The compounds were extruded into filament by using filament extruder. The two temperature profiles were used. The first and the second temperature profiles from the feed zone to the die zone were 275-275-275 oC and 290-290-290 oC, respectively. The extrudate of modified-rPET with and without heat stabilizer, were investigated the type of gel and the thermal behavior of the modified-rPET filament. From this preliminary experiment, it was found that the “unmelt-gel” defect was found from the modified-rPET filament, without the addition of Irganox®1010. On the other hand, the “crosslinked gel” defect was found from the modified-rPET filament, with the addition of Irganox®1010. Therefore, the addition of heat stabilizer (Irganox®1010) may cause the “crosslinked gel” significantly. Our future work, we will investigate the effect of another stabilizer and chain extenders on the gelation behavior, to complete this clarification systematically.

Electrochemical Nanoimprinting of Colored Infrared Reflective Patterns for Radiative Heating

AbstractMetallic nanostructures hold immense promise for radiative heating technology because of their distinctive capability to simultaneously achieve high mid‐infrared reflectance and generate vibrant colors through structural or plasmonic effects. However, fabricating metallic nanostructures remains challenging using traditional top–down techniques. Here, the solid‐state superionic stamping (S4) process is demonstrated as a scalable and economical tool to electrochemically imprint metallic grid nano‐patterns onto flexible substrates. With precise control over grid width and length at the nanoscale, the S4 approach enables the fabrication of nano‐patterned grid coatings exhibiting a spectrum of colors. These coatings also show high mid‐infrared reflectance exceeding 80% at 9.5 µm, leading to radiative heating effects of 5.9 and 3.1 °C compared to bare skin and cotton, respectively. This work introduces a viable strategy for creating colored infrared‐reflective patterns, paving the way for diverse thermal management applications.

Gecko-inspired adhesion enhanced by electroadhesive forces

Abstract Soft robotic manipulators have been increasingly adopted over the last decade due to their passive conformation to the shapes of objects, which can reduce control complexity. The performance of these grippers can be improved using flexible adhesive skins that increase tactile gripping forces, which is particularly important when grasping delicate objects and flexible substrates that are otherwise difficult to manipulate. In this work, we investigate how passive gecko-inspired fibrillar adhesion can be augmented by actively controlled electroadhesion (EA). The passive gecko-inspired outer skin (GS) enables adhesion with no power consumption while EA is controlled with an applied voltage. A numerical finite-element model is used to investigate how EA is affected by a commercially available gecko-inspired skin. The results show that the dielectric properties of the gecko-inspired skin reduce the magnitude of field intensity on the adhesive contact surface by only 2.1% at 3 kV. Compared with GS alone, EA with gecko-inspired skin (EAGS) increases the shear force by 66.8% and the normal force by 53.7% with an applied voltage of 4 kV. It is shown that the gecko skin’s adhesion force is enhanced by increased engagement of the fibrillar microstructure to object surfaces due to EA. This is experimentally demonstrated using frustrated total internal reflection imaging. This work shows that electroadhesive-enhanced gecko-inspired skin generates a greater adhesive force than the sum of forces from the separate gecko-inspired skin and EA. In this way, electrically controllable and passive adhesion mechanisms can be combined to improve the handling of flexible and delicate objects with smooth or rough surfaces.

Frequency Selective Surfaces: Design, Analysis, and Applications

This paper aims to provide a general review of the fundamental ideas, varieties, methods, and experimental research of the most advanced frequency selective surfaces available today. Frequency-selective surfaces are periodic structures engineered to work as spatial filters in interaction with electromagnetic (EM) waves with different frequencies, polarization, and incident angles in a desired and controlled way. They are usually made of periodic elements with dimensions less than the operational wavelength. The primary issue examined is the need for more efficient, compact, and adaptable electromagnetic filtering solutions. The research method involved a comprehensive review of recent advancements in FSS design, focusing on structural diversity, miniaturization, multiband operations, and the integration of active components for tunability and reconfigurability. Key findings include the development of highly selective miniaturized FSSs, innovative applications on flexible and textile substrates, and the exploration of FSSs for liquid and strain sensing. The conclusions emphasize the significant potential of FSS technology to enhance wireless communication, environmental monitoring, and defense applications. This study provides valuable insights into the design and application of FSSs, aiming to guide future research and development in this dynamic field.

Exploring the Potential of Recycled Polyethylene Terephthalate—Lignocellulose/Carbon Nanotube–Graphene Nanosheets an Efficient Extractor for Oil Spill

The global challenge of oil spill treatment has been addressed using nanocomposite-based natural fibers. These materials offer great potential in oil spill cleanup and are considered due to their environmental friendliness, high efficiency, and low cost. Thus, the current study reports a novel composite fabricated from date palm fiber (DPF) and recycled polyethylene terephthalate (rPET) with a proper combination of a mixture of carbon nanotubes (CNTs) and graphene nanosheets (GNSs) for oil removal. The established nanocomposite (DPF-rPET/CNT/GNS) was fabricated via physical mixing of various quantities (0.9, 0.8, and 0.7 g) of PET, along with varying loads of DPF at different proportions of CNT:GNS. The prepared nanocomposite (DPF-rPET/CNT/GNS) was fully characterized using scanning electron microscopy–energy dispersive X-ray (SEM-EDX) analysis, transmission electron microscopy (TEM), thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FTIR), and Brunauer–Emmett–Teller (BET) analysis. In static experiments and under the optimal parameters of pH, sorbent doze, shaking time, and quantity of diesel oil), the established sorbent (DPF-rPET/CNT-GNS nanocomposite) displayed excellent adsorption capacity (98 mg/g). This study also expands the utility of the sorbent for the reusability of the oil adsorption, maintaining performance after five cycles. The adsorption data fitted well with the Langmuir isotherm model with a correlation coefficient (R2) of 0.99 and maximum adsorption capacity of 99.7 mg/g, indicating monolayer adsorption. Additionally, the adsorption kinetics followed a pseudo-second-order model, with an R2 near unity and an adsorption capacity of 99.09 mg/g. This study highlights the promising potential of the DPF-rPET/CNT-GNS composite as an effective adsorbent for treating oily water.

Enhancing shelf-life and nutritional value of broccoli florets through vacuum impregnation with calcium chloride and ascorbic acid.

The present investigation aimed to enhance the postharvest shelf-life of broccoli using vacuum impregnation (VI). Broccoli florets were impregnated with physiologically active chemicals, i.e. calcium chloride and ascorbic acid. Post-impregnation broccoli florets were packed in three different packaging materials (poly(ethylene terephthalate) punnets, low-density polyethylene pouches and shrink-wrap film) and stored at two temperatures (5 and 25 °C). The effects of impregnation solutions, packaging materials and storage temperature on physicochemical attributes (weight loss, total soluble solids, ascorbic acid, total chlorophylls and carotenoid content), antioxidant and phenolic contents, and shelf life were studied. The changes in the chemical structure post-impregnation and during storage were investigated using Fourier transform infrared (FTIR) spectroscopy. Results showed that impregnated broccoli florets exhibited significantly (P < 0.05) higher levels of biochemical attributes immediately after impregnation. During storage, the physicochemical and antioxidant properties of broccoli florets declined for all the samples. However, the reduction in these properties was significantly (P < 0.05) lower in impregnated florets as compared to untreated control samples. Principal component analysis and FTIR results also indicated a clear difference in the impregnated and control samples. The shelf-life of broccoli florets stored at 25 °C was assessed as 4 and 3 days for impregnated and control samples, respectively; whereas the samples stored at 5 °C had a shelf-life of 12 days for impregnated samples and 5 days for the control samples. The findings of the study elucidate the potential of VI in enhancing the initial quality and shelf-life of broccoli. The deterioration during storage is primarily due to physiological weight loss, a natural loss of water and volatile compounds that occur following harvest due to transpiration and respiration. Excessive transpiration can lead to dehydration, which reduces the quality and shelf-life of the product. © 2024 Society of Chemical Industry.

Hydrogenating Polyethylene Terephthalate into Degradable Polyesters

The recycling and upcycling of polyethylene terephthalate (PET), the most widely used polyester plastic globally, has attracted growing attention concerning its disposal as non‐degradable waste in the natural environment. Transforming end‐of‐life PET into (bio)degradable polyester offers a novel approach to managing its waste. In this study, we introduce a simple process capable of converting waste PET into degradable polyester, polyethylene terephthalate‐polyethylene‐1,4‐cyclohexanedicarboxylate (PET‐PECHD), by partly hydrogenating the aromatic rings (x) into aliphatic ones (y). The polyesters with variable x/y compositions ranging from 100/0 to 0/100 can be achieved, and the molecular weight (Mw) can be maintained when x/y &gt; 87/13 due to the nonobvious depolymerization. Pronounced depolymerization would occur with deeper hydrogenation, which generates a blend of PET‐PECHD and polyethylene‐1,4‐cyclohexanedicarboxylate (PECHD) with lower Mw, and finally a single‐type polymer PECHD. The PET‐PECHD demonstrates comparable thermal stability and mechanical strength compared to PET, along with superior extensibility, barrier properties, and (bio)degradability in acidic, alkaline solutions, and moist soil. This research highlights the potential for cost‐effective, large‐scale production of degradable polyester from real‐life plastic waste.

Hydrogenating Polyethylene Terephthalate into Degradable Polyesters.

The recycling and upcycling of polyethylene terephthalate (PET), the most widely used polyester plastic globally, has attracted growing attention concerning its disposal as non-degradable waste in the natural environment. Transforming end-of-life PET into (bio)degradable polyester offers a novel approach to managing its waste. In this study, we introduce a simple process capable of converting waste PET into degradable polyester, polyethylene terephthalate-polyethylene-1,4-cyclohexanedicarboxylate (PET-PECHD), by partly hydrogenating the aromatic rings (x) into aliphatic ones (y). The polyesters with variable x/y compositions ranging from 100/0 to 0/100 can be achieved, and the molecular weight (Mw) can be maintained when x/y > 87/13 due to the nonobvious depolymerization. Pronounced depolymerization would occur with deeper hydrogenation, which generates a blend of PET-PECHD and polyethylene-1,4-cyclohexanedicarboxylate (PECHD) with lower Mw, and finally a single-type polymer PECHD. The PET-PECHD demonstrates comparable thermal stability and mechanical strength compared to PET, along with superior extensibility, barrier properties, and (bio)degradability in acidic, alkaline solutions, and moist soil. This research highlights the potential for cost-effective, large-scale production of degradable polyester from real-life plastic waste.

Mechanical characterization of a 3D printed lattice core sandwich structure

AbstractSandwich structures have garnered interest as versatile structures for applications in advanced engineering structures. To fabricate sandwich structures, plastics have replaced conventional materials; however, most of these plastics remain in the environment beyond their functional lifespan. This study describes the fabrication of sustainable hybrid sandwich structures with 3D printed poly‐lactic acid (PLA) cores and self‐reinforced polyethylene terephthalate (srPET) face sheets. The mechanical responses of the hybrid sandwich structures with three types of lattice cores, S‐90, S‐45, and S‐V, were compared with those of the parent material sandwich structures after performing bending and impact tests. The face sheet in the hybrid sandwich structure transferred the load to the core without failure. The hybrid sandwich structure containing the S‐90 core exhibited a higher fracture strength (52.4 MPa) and tangent modulus of elasticity (2860 MPa) than those of the other structures. S‐V exhibited the highest fracture strains of 3.3% and 5% for parent material and hybrid sandwich structures, respectively. This study highlights the sandwich structures with excellent mechanical properties for structural applications.Highlights Novel sandwich structures with 3D printed PLA cores are fabricated. Three‐point bending and low‐velocity impact tests are performed. Failure occurred in the core, but the Sr‐PET face sheets did not deform. Hybrid sandwich structures significantly improve mechanical performance.

Clickable Plastic Surfaces with Controllable Azide Surface Density

AbstractThis study investigates the surface functionalization of plastic substrates through dip‐coating in azide‐functionalized polymer solutions, followed by a click reaction (i.e., strain‐promoted azide–alkyne cycloaddition). Acrylic, poly(ethylene terephthalate) (PET), and nylon substrates are dip‐coated with a series of polymers containing various azide groups grafted onto the poly(methyl methacrylate‐co‐hydroxyethyl methacrylate) backbone to examine structural effects on the surface density of clickable azide groups. X‐ray photoelectron spectroscopy and fluorescence spectroscopy confirm the subsequent click‐immobilization of cycloalkyne‐tagged fluorescein, which is quantified to calculate the surface density of clickable azide groups. Further investigations demonstrate that the surface density of azide groups can be controlled by manipulating the polymer ratio during dip‐coating, thus enabling the preparation of a linear surface gradient in terms of azide group density. Finally, the microcontact printing (µCP) method is employed to pattern the functionalized surfaces and quantify the functional molecules immobilized on the surface by µCP. This study highlights the adaptability of click chemistry and polymer coating techniques for the advanced functionalization of plastic surfaces for materials science and engineering applications.