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PET
APPLIED SURFACE SCIENCE · 2016 · IF 3.15

A novel and simple method of printing flexible conductive circuits on PET fabrics

Zehong Wang,Wei Wang,Zhikang Jiang,Dan Yu

Flexible conductive circuits on PET fabrics were fabricated by a simple approach. Firstly, well dispersed nano-silver colloids with average size of 87   nm were synthesized with poly (vinyl pyrrolidone). Then, by adding polyurethane and thickening agent into these colloids, Ag NP-based ink was produced and printed on PET fabrics by screen printing. Conductive patterns were achieved through the swelling process of polyurethane and the decrease of contact resistance between nano-silver particles when immersed in dichloromethane (DCM) and diallyldimethylammonium chloride (DMDAAC) mixed solution. After it was dried at 40   °C,the surface resistivity was about 0.197   Ω   cm with width 1.9   mm, and thickness 20   μm. Moreover, the effects of different DCM contents on the conductivity and the film forming ability have been investigated. We believe these foundings will provide some important analysis for printing flexible conductive circuits on textiles.

研究领域: 材料科学 · 纺织工程 · 电子制造
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Frontiers in Oncology · 2022 · IF 5.738

Preclinical evaluation and first in human study of Al18F radiolabeled ODAP-urea-based PSMA targeting ligand for PET imaging of prostate cancer

Ren Ya’nan,Liu Chen,Liu Teli,Duan Xiaojiang,Zhang Qian,Liu Jiayue,Wang Pei,Guo Qian,Yang Xing,Du Peng,Zhu Hua,Yang Zhi

Purpose: This study aimed to introduce a novel [18F]AlF-labeled ODAP-Urea-based Prostate-specific membrane antigen (PSMA) probe, named [18F]AlF-PSMA-137, which was derived from the successful modification of glutamate-like functional group. The preclinically physical and biological characteristics of the probe were analyzed. Polit clinical PET/CT translation was performed to analyze its feasibility in clinical diagnosis of prostate cancer.Methods: [18F]AlF-PSMA-137 was maturely labeled with the [18F]AlF2+ labeling technique. It was analyzed by radio-HPLC for radiochemical purity and stability analysis in vitro and in vivo. The PSMA specificity was investigated in PSMA-positive (LNCaP) and PSMA-negative (PC3) cells, and the binding affinity was evaluated in LNCaP cells. Micro-PET/CT imaging was performed in mice bearing LNCaP or PC3 tumors. Thirteen patients with newly diagnosed prostate cancer were included for [18F]AlF-PSMA-137 PET/CT imaging. Physiologic biodistribution and tumor burden were semi-quantitatively evaluated and the radiation dosimetry of [18F]AlF-PSMA-137 was estimated.Results: The radiochemical yield of [18F]AlF-PSMA-137 was 54.2 ± 10.7% (n = 16) with the radiochemical purity over 99% and the specific activity of 26.36 ± 7.33 GBq/μmol. The binding affinity to PSMA was 2.11 ± 0.63 nM. [18F]AlF-PSMA-137 showed high cell/tumor uptake which can be specifically blocked by PSMA inhibitor. According to the biodistribution in patients, [18F]AlF-PSMA-137 was mainly accumulated in kidneys, lacrimal glands, parotid glands, submandibular glands and liver which was similar to the extensive Glu-Ureas based probes. A total of 81 lesions were detected in PET/CT imaging and over 91% of lesions increased between 1 h p.i. (SUVmean: 10.98 ± 18.12) and 2 h p.i. (SUVmean: 14.25 ± 21.28) (p < 0.001). Additionally, the probe showed intensive accumulation in lesions which provided excellent imaging contrast with the high tumor-to-muscle ratio of 15.57 ± 27.21 at 1 h p.i. and 25.42 ± 36.60 at 2 h p.i. (p < 0.001), respectively. The effective dose of [18F]AlF-PSMA-137 was estimated as 0.0119 ± 0.0009 mSv/MBq.Conclusion: An ODAP-Urea-based PSMA probe [18F]AlF-PSMA-137 was successfully prepared with high specificity and binding affinity to PSMA. Micro-PET/CT imaging study demonstrated its feasibility for prostate cancer imaging. Pilot clinical study showed its potential for delay-imaging and prostate cancer detection.

CAS / MDL: 76-05-1
研究领域: 医学影像学 · 肿瘤学 · 放射化学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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APPLIED CATALYSIS A-GENERAL · 2025 · IF 4.8

Upgrading of PET to CHDM over base metal catalysts via tandem processes

Wanzhen Ren,Chuan Gang,Chen Zhao,Peng Wu,Xiaohong Li

1,4-cyclohexanedimethanol (CHDM), which has similar structural units to PET (polyethylene terephthalate), is a crucial polyester monomer. Therefore, PET can be directly oriented to synthesize CHDM through tandem alcoholysis and selective hydrogenation. However, use of precious metal catalysts such as Pd or Ru catalyst limits the industrial application. Herein, we developed a new process that converts PET into CHDM in mixed solvent of CH 3 OH-1,4-dioxane via tandem three-step reactions without the involvement of precious metal catalysts or any separation or purification, including the methanolysis of PET to obtain dimethyl terephthalate (DMT) first, then DMT was hydrogenated over a NiLa-40wt% catalyst to form the intermediate dimethyl 1,4-cyclohexanedicarboxylate (DMCD), followed by the further hydrogenolysis of DMCD to CHDM over a Cu 1 Fe 1 Al 0.5 catalyst to yield CHMD with an overall CHDM yield of .90.2 %. Importantly, the final product CHDM could be separated easily just by distillation because there is a significant difference in the boiling point of CHDM with the by-products.

研究领域: 化学工程 · 催化科学 · 材料科学
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Journal of Environmental Chemical Engineering · 2022 · IF 7.968

Rapid alcoholysis of PET enhanced by its swelling under high temperature

Pengtao Fang,Shuqian Xia,Xingmei Lu

The development of catalysts with high thermal stability, high catalytic activity and high cycling performance has been an important challenge in PET alcoholysis research. PET degradation is a surface interface controlled process, but PET as a dense solid with lower specific surface area severely reduces its degradation rate. Here, the high specific surface area (0.4–3.3 m 2 /g) and the large number of pores (0–17.5 nm) formed by the swelling of PET at high temperature were used to break the interfacial confinement between the reactants; then the rapid and complete degradation of PET was achieved under the multi-hydrogen bonding microenvironment formed by the multi-active site polyoxometalate (POM) catalysts K 10 [M 4 (H 2 O) 2 (PW 9 O 34 ) 2 ]-H 2 O (M = Zn, Mn, Cu, Ni, Co) and EG. Finally, accompanied by the attack of the transition metal active site on C O of PET, 1.0 g of PET could be completely degraded in 5 min under the optimal reaction conditions (2.0 wt% of catalyst to PET, 240 °C) and the bis(hydroxyethyl) terephthalate (BHET) yield of 92.8% was achieved within 8 min. Moreover, the catalyst could be recycled more than 30 times, which is very meaningful. In the same time, the mechanism of PET alcoholysis was investigated and proposed a mechanism of PET alcoholysis.

研究领域: 化学工程 · 材料科学 · 催化反应
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Catalysis Science & Technology · 2023 ·Vol. 13 ·期 22 ·6561-6569 · IF 5

Efficient depolymerization of PET over Ti-doped SBA-15 with abundant Lewis acid sites via glycolysis

Songlei Mo,Yong Guo,Xiaohui Liu,Yanqin Wang

The glycolysis of polyethylene terephthalate (PET) is considered as the most promising PET recycling strategy due to its mild reaction conditions and circularity. Herein, several metal-doped SBA-15 (M/SBA-15) as heterogeneous Lewis acid catalysts were investigated to screen the best catalyst and to understand the essence for their differences in PET glycolysis. It is found that the catalytic activity is positively correlated with the acid amount in different metal-doped SBA-15 and Ti/SBA-15 with different Ti loadings, with the exception of Nb/SBA-15. 4Ti/SBA-15 with abundant Lewis acid sites shows excellent PET glycolysis ability, with the yield of bis(2-hydroxyethyl) terephthalate (BHET) reaching 87.2% within 45 min at 190 °C (isolated yield 73%). While 4Nb/SBA-15 has a similar acid amount as that in 4Ti/SBA-15, but it has very low catalytic activity probably due to its strong oxygen affinity. Acetone–methanol-adsorption DRIFTS confirms its strong oxygen affinity, which would poison the acid sites by ethylene glycol (EG) and result in very low activity. This study demonstrates that PET glycolysis activity is really correlated with the amount of Lewis acid sites, but species with very strong oxygen affinity would lower its activity. Further diffuse reflection ultraviolet-visible (DR UV-vis) spectra analysis confirms that tetrahedral Ti4+ species in Ti/SBA-15 is the real active center. In addition, 4Ti/SBA-15 has good reusability and can be used in common real PET (dyed polyester fabric, PET bottles) glycolysis. These results indicate that increasing the amount of Lewis acid sites is a promising way to enhance PET glycolysis and 4Ti/SBA-15 with high activity and stability is a potential catalyst for industrial application.

研究领域: 材料科学 · 催化化学 · 环境科学
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2020 · IF 3.232

“Turn-on” fluorescent sensor for Th4+ in aqueous media based on a combination of PET-AIE effect

Shibing Chen,Shengjie Jiang,Hongyu Guo,Fafu Yang

Previously reported fluorescent sensors for Th 4+ experienced emission quenching or generated false positive signal upon aggregate formation in aqueous media. Herein, a simple and novel thorium sensor ( CDB-BA ) based on cyanodistyrene structure was designed and synthesized, which integrated the highly emitting characteristic of AIE effect and off-on response of PET modulation for the first time to construct the “turn-on” fluorescent probe for Th 4+ . Besides excellent selectivity, CDB-BA exhibited remarkable fluorescent enhancement which was linearly related to the concentration of Th 4+ in the range of 0.25–8 μM. The detection limit was attained 0.074 μM, which was lower than that of most previously reported sensors. The mechanism of tris-chelate complex of CDB-BA with Th 4+ was confirmed by mass spectra, IR spectra and DFT calculation. The excellent Th 4+ sensing ability of CDB-BA was successfully applied to detecting Th 4+ on TLC plates, in real water samples and living-cell imaging. This work suggested that the combination of AIE and PET photophysical mechanism could offer the merits of minimized background and enhanced signal fidelity to develop novel “turn-on” fluorescent probe in complicated aqueous environment and biological research.

研究领域: 化学 · 生物医学
✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF POLYMER SCIENCE · 2024 · IF 3.9

Silica-Coated Hybrid Perovskite Catalysts for Well-Controlled PET-RAFT Polymerization in Polar Solvents

Weijie Zhang,Yuxiang Zhang,Jingjing Xiao,Xiaowei Wang,Lei Liu,Jibin Han,Hui Wang,Anchao Feng

Lead halide perovskite has currently emerged as a research hotspot in the field of photocatalysis due to its exceptional photovoltaic characteristics. Despite its potential, the susceptibility to degradation under harsh conditions such as light, humidity, and polar solvents poses a significant challenge. To counteract this, a strategy employing silica to shield the perovskite surface is conducted, thereby enhancing its stability. The resulting composite MAPbBr 3 @SiO 2 is then deployed as a photocatalyst in the photoinduced electron/energy transfer reversible addition fragmentation chain transfer (PET-RAFT) polymerization of butyl acrylate within polar solvents. The catalytic performance across different RAFT polymerization systems including varying the RAFT reagents, catalyst concentrations, and solvent types is meticulously examined. Remarkably, with a photocatalyst loading of merely 0.004 wt% and under a blue light intensity of 6 mW/cm 2 , over 80% monomer conversion can be achieved in 4 h. Moreover, the molecular weight distribution ( Đ ) consistently remains within the narrow range of 1.0–1.2 across all experimental setups, which proves the controllable nature of the PET-RAFT process. Owning the advantages of low photocatalyst requirement, compatibility with polar solvents, and narrow molecular weight distribution, PET-RAFT polymerization mediated by MAPbBr 3 @SiO 2 holds promise for scalable manufacturing and industrial-scale applications. Graphical Silica-coated hybrid lead halide perovskite nanocrystals are prepared and applied as photocatalysts in a PET-RAFT polymerization within polar solvents. High monomer conversion rates and polymers with narrow molecular weight distribution can be achieved. The polymerization process is notably efficient and can be conducted with minimal photocatalyst amounts, underscoring the superior efficiency and broad applicability of our novel photocatalyst system.

CAS / MDL: 71-23-8
研究领域: 材料科学 · 高分子化学 · 光催化领域
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ACS Applied Materials & Interfaces · 2022 · IF 10.383

Novel Transparent TiO2/AgNW–Si(NH2)/PET Hybrid Films for Flexible Smart Windows

Tingting Hao,Shen Wang,Hongbo Xu,Xiang Zhang,Shlomo Magdassi,Lei Pan,Ying Song,Yao Li,Jiupeng Zhao

The application of flexible indium tin oxide (ITO)-free electrochromic devices (FCDs) has always been a research hotspot in flexible electronics. Recently, a silver nanowire (AgNW)-based transparent conductive film has raised great interest as an ITO-free substrate for FCDs. However, several challenges, such as the weak binding of AgNWs to the substrate, high junction resistance, and oxidation of AgNWs, remain. In this paper, a novel method for surface modification of AgNWs with N-aminoethyl-γ-aminopropyltrimethoxysilane [Si(NH2)] solution is proposed to enhance the bonding with the flexible substrates and the active materials, thereby inhibiting the delamination of AgNWs from the substrate and reducing the high junction resistance between nanowires. The TiO2/AgNW–Si(NH2)/poly(ethylene terephthalate) (PET) films show outstanding mechanical properties, of which the resistance remains almost unchanged after mechanical bending of 5000 cycles (ΔR/R0 ≈ 3.6%) and repeated peeling off cycles with 3M tape 100 times (ΔR/R0 ≈ 6.0%). In addition, we found that the oxygen-containing groups on the TiO2/AgNW–Si(NH2)/PET surface form hydrogen bonds with the TiO2 sol, resulting in tight contact between the TiO2 sol and the AgNWs, which prevents the AgNWs from oxidation. As a result, the TiO2/AgNW–Si(NH2)/PET film exhibited long-time aging (ΔR/R0 ≈ 4.9% in the air for 100 days) stability. A FCD was constructed with the TiO2/AgNW–Si(NH2)/PET film, which showed excellent electrochromic performance (94% retention) after 5000 bending cycles, indicating high stability and mechanical flexibility. These results present a promising solution to the transparent conductive films for flexible energy devices.

研究领域: 材料科学 · 柔性电子技术
✓ 已验证 DOI PubMed 高影响因子
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Polymers · 2019 ·Vol. 11 ·期 3 ·520 · IF 3.164

Mechanism of Accelerant on Disperse Dyeing for PET Fiber in the Silicone Solvent Dyeing System

Jiping Wang,Wenqing Cheng,Yuanyuan Gao,Lei Zhu,Liujun Pei

Disperse dyeing for polyethylene terephthalate (PET) fiber in different non-aqueous solvent dyeing systems have been extensively studied over the past decades. In the present work, disperse dyeing for PET was investigated in a silicone solvent dyeing system. The influence of accelerant on the fiber swelling, uptake of dye, K/S value of dyed fiber, and dye solubility in the silicone solvent were systematically investigated. Compared with no accelerant, the final uptake of the disperse dye (C. I. Disperse Blue 367) could increase to 81% with 20% accelerant in the silicone solvent dyeing system, and the K/S value of dyed fiber was also higher (3.3 for no accelerant vs. 13.2 for accelerant). The influence of accelerant on the performance of disperse dyeing was also studied. Firstly, the solubility of the disperse dye in the silicone solvent can be decreased by the accelerant. Moreover, the solubility of the disperse dye is inversely proportional to the K/S value and the uptake of the dye. In addition, although the silicone solvent can diffuse to the inner fiber and has a partial swelling in the PET fiber, the swelling of PET can be improved by the accelerant. Furthermore, the swelling of fiber can reach equilibrium when the amount of accelerant was 15% (the weight of fiber). Therefore, this eco-friendly dyeing technology has considerable potential for application to a broad array of chemical fibers.Keywords:PET fiber;disperse dye;silicone solvent;accelerant;solubility;swelling

研究领域: 纺织化学 · 材料科学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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Pharmaceuticals · 2022 ·Vol. 15 ·期 5 ·513 · IF 5.215

An Albumin-Binding PSMA Ligand with Higher Tumor Accumulation for PET Imaging of Prostate Cancer

Ya’nan Ren,Teli Liu,Chen Liu,Xiaoyi Guo,Feng Wang,Hua Zhu,Zhi Yang

Prostate-specific membrane antigen (PSMA) is an ideal target for the diagnosis and treatment of prostate cancer. Due to the short half-life in blood, small molecules/peptides are rapidly cleared by the circulatory system. Prolonging the half-life of PSMA probes has been considered as an effective strategy to improve the tumor detection. Herein, we reported a64Cu-labeled PSMA tracer conjugating with maleimidopropionic acid (MPA),64Cu-PSMA-CM, which showed an excellent ability to detect PSMA-overexpressing tumors in delayed time. Cell experiments in PSMA-positive 22Rv1 cells, human serum albumin binding affinity, and micro-PET imaging studies in 22Rv1 model were performed to investigate the albumin binding capacity and PSMA specificity. Comparisons with64Cu-PSMA-BCH were performed to explore the influence of MPA on the biological properties.64Cu-PSMA-CM could be quickly prepared within 30 min. The uptake of64Cu-PSMA-CM in 22Rv1 cells increased over time and it could bind to HSA with a high protein binding ratio (67.8 ± 1.5%). When compared to64Cu-PSMA-BCH,64Cu-PSMA-CM demonstrated higher and prolonged accumulation in 22Rv1 tumors, contributing to high tumor-to-organ ratios. These results showed that64Cu-PSMA-CM was PSMA specific with a higher tumor uptake, which demonstrated that MPA is an optional strategy for improving the radioactivity concentration in PSMA-expressing tumors and for developing the ligands for PSMA radioligand therapy.Keywords:PSMA;prostate cancer;copper radioisotopes;maleimidopropionic acid;PET imaging

CAS / MDL: 76-05-1
研究领域: 医学影像学 · 肿瘤学 · 放射化学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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JOURNAL OF HAZARDOUS MATERIALS · 2022 · IF 14.224

Directional-path modification strategy enhances PET hydrolase catalysis of plastic degradation

Xiao-Qian Chen,Zhi-Yong Guo,Lei Wang,Zheng-Fei Yan,Chang-Xu Jin,Qing-Song Huang,De-Min Kong,De-Ming Rao,Jing Wu

Poly (ethylene terephthalate) (PET) is a widely used type of general plastic that produces a significant amount of waste due to its non-degradable properties. We propose a novel directional-path modification (DPM) strategy, involving positive charge amino acid introduction and binding groove remodeling, and apply it to Thermobifida fusca cutinase to enhance PET degradation. The highest value of PET degradation (90%) was achieved in variant 4Mz (H184S/Q92G/F209I/I213K), exhibiting values almost 30-fold that of the wild-type. We employed molecular docking, molecular dynamics simulations, and QM/MM MD for the degradation process of PET, accompanied by acylation and deacylation. We found that the distance of nucleophilic attack was reduced from about 4.6 Å in the wild type to 3.8 Å in 4Mz, and the free energy barrier of 4Mz dropped from 14.3 kcal/mol to 7.1 kcal/mol at the acylation which was the rate-limiting step. Subsequently, the high efficiency and universality of the DPM strategy were successfully demonstrated in LCC, Est119, and BhrPETase enhancing the degradation activity of PET. Finally, the highest degradation rate of the pretreated commercial plastic bottles had reached to 73%. The present study provides insight into the molecular binding mechanism of PET into the PET hydrolases structure and proposes a novel DPM strategy that will be useful for the engineering of more efficient enzymes for PET degradation.

研究领域: 生物化学 · 环境科学
✓ 已验证 DOI PubMed 高影响因子
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Polymers · 2019 ·Vol. 11 ·期 5 ·892 · IF 3.164

PET-RAFT Polymerization Catalyzed by Small Organic Molecule under Green Light Irradiation

Huazhen Tao,Lei Xia,Guang Chen,Tianyou Zeng,Xuan Nie,Ze Zhang,Yezi You

Photocatalyzed polymerization using organic molecules as catalysts has attracted broad interest because of its easy operation in ambient environments and low toxicity compared with metallic catalysts. In this work, we reported that 4,7-di(thiophen-2-yl)benzo[c][1,2,5]thiadiazole (DTBT) can act as an efficient photoredox catalyst for photoinduced electron transfer-reversible addition-fragmentation chain transfer (PET-RAFT) polymerization under green light irradiation. Well-defined (co)polymers can be obtained using this technique without any additional additives like noble metals and electron donors or acceptors. The living characteristics of polymerization were verified by kinetic study and the narrow dispersity (Đ) of the produced polymer. Excellent chain-end fidelity was demonstrated through chain extension as well. In addition, this technique showed great potential for various RAFT agents and monomers including acrylates and acrylamides.Keywords:organic photoredox catalyst;green light;PET-RAFT polymerization

研究领域: 高分子化学 · 材料科学
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