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CELLULOSE · 2024 · IF 4.9

Cotton fabric with durable flame retardancy, robust superhydrophobicity and reliable UV shielding

Zhou Canhao,Ma Yongqiang,Rong Hui,Yu Xinghui,Liu Siyuan,Deng Liandong,Zhang Jianhua,Li Shuangyang,Dong Anjie

A new strategy for multifunctional coatings with flame retardancy, superhydrophobicity and UV shielding ability on cotton fabrics (SFR cotton) was realized by step-by-step spraying ammonium phytate, lignin and hybrid nanoparticles of polydimethylsiloxane (PDMS) modified mesoporous silica nanoparticles (MSNs) with entrapped Fe 2 O 3 (PDMS@Fe 2 O 3 -MSNs). The surface adhesion PDMS@Fe 2 O 3 -MSNs constructed micro/nano-scale surface structure on SFR cotton fabric, which endowed superhydrophobic (WCA = 152 ± 1.3°), anti-fouling and self-cleaning properties. Benefiting from the synergistic effects of the physical barrier provided by the PDMS@Fe 2 O 3 -MSNs and the intumescent flame-retardant properties of ammonium phytate and lignin, the SFR cotton fabric demonstrated excellent self-extinguishing performance under an open fire and left a char layer with 8.4 cm. In addition, due to the excellent UV-absorption ability of lignin and Fe 2 O 3 nanoparticles, the SFR cotton fabric was able to shield the UV irradiation damages to rat skin. Furthermore, the SFR cotton fabric demonstrated remarkable durability against rigorous conditions, including ultrasonic washing, sandpaper abrasion, UV irradiation and exposure to strong acid/alkali environments. After 150 min of ultrasonic washing and 50 cycles of abrasion, the SFR cotton fabric could preserve its hydrophobicity, flame retardancy and UV shielding ability. In addition, the SFR cotton fabric delivered exceptional chemical stability and UV durability when exposed to strong acid/alkali for 24 h and UV irradiation (200 W) for 12 h, respectively. Significantly, the SFR cotton fabric could retain the original flexibility and breathability of pristine cotton fabric. Therefore, the simple and feasible strategy of multifunctional coatings has broad application prospects in advanced multifunctional textiles, military facilities and other fields.

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Water Reuse · 2024 ·Vol. 14 ·期 3 ·384-395 · IF 4.3

Degradation of acetochlor via the UV/persulfate process: Mechanisms, kinetics, and pathways

Hu Chen-Yan,Ji Sheng-Jie,Dong Zheng-Yu,Wu Yi-Hui,Dong Zi-Yi,Hu Li-Li,Yang Xin-Yu,Liu Hao

View large Download slide View large Download slide Close modal The environmental health risks of acetochlor (ACE) have received widespread attention. The removal of ACE via the ultraviolet/persulfate (UV/PS) process was investigated in this study. The degradation of ACE in the UV/PS process fitted pseudo-first-order kinetics. ACE can be effectively removed in the pH range of 5.0–9.0. In addition, the removal efficiency of ACE increases with the increase in PS concentration. The experimental and calculation results prove that the contributions of UV irradiation, sulfate radicals (SO 4 •- ) and hydroxyl radicals (HO·) were 40, 52.1, and 6.43%, respectively, and the second-order rate constants between SO 4 •- and with ACE are 3.5 × 10 9 and 5.6 × 10 9 M −1 s −1 , respectively. The influences of different water matrices were explored. Both chloride ions and bicarbonate can inhibit the degradation of ACE, while the effects of sulfate ions and nitrate can be negligible. Humic acid (HA) has an inhibitory effect of ACE degradation. The intermediates were detected and the possible degradation pathway of ACE was proposed. The results of this study can provide technical support for the control of ACE in the environment. The degradation of acetochlor in the UV/PS process was investigated. The kinetic model of acetochlor degradation in the UV/PS process was proposed. Both UV irradiation, SO 4 •- , and are involved in the degradation of acetochlor. The degradation pathway of acetochlor was proposed in the UV/PS process.

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Journal of Water Process Engineering · 2024 · IF 6.3

Degradation of organophosphate esters by UV/persulfate: Kinetic, mechanistic and toxicity evaluation

Xin Chen,Saier Wang,Lianghu Su,Jun Zhang,Huiming Xiang

With the ban of brominated flame retardants , organophosphate esters (OPEs) have been widely used. The ultraviolet combined sodium persulfate (UV/PS) process is a promising advanced oxidation process (AOPs), which effectively removes organic micropollutants by generating various reactive substances such as hydroxyl radical (•OH) and sulfate radical (SO• 4 − ). The degradation kinetics, influencing factors, degradation path, and toxicity of three organic phosphates , trimethyl phosphate (TMP), tris (2-chloroethyl) phosphate (TCEP) and triphenyl phosphine oxide (TPPO) were studied. The results showed that UV/PS could degrade OPEs efficiently, and 254 nm UV light was more conducive to the degradation of OPEs than 365 nm UV light, and the degradation of OPEs accelerated with the increase of PS concentration. Under acidic and neutral conditions, UV/PS was more conducive to the degradation of OPEs, and the concentration of NOM was inversely proportional to the degradation rate of OPEs, Cl − and SO 4 2− had almost no effect on the degradation of OPEs, while HCO 3 − has an inhibitory effect on the degradation of OPEs. UV/PS also has a good effect on the degradation of OPEs in actual water. •OH and SO• 4 − , as the main reactive radicals, participate in the degradation of OPEs. Hydroxylation , debenzene ring, demethylation , and ring opening reactions are the main reactions occurring in the process of OPEs degradation. The theoretical toxicity value of most intermediates is lower than that of the initial OPEs. This study reveals the transformation of OPEs in the UV/PS system and provides a new idea for wastewater treatment of OPEs.

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Physica Status Solidi-Rapid Research Letters · 2024 · IF 2.5

Epitaxial Growth of Cs3Cu2I5 Single-Crystal Arrays for UV-Responsive Neuromorphic Devices

Yang Yu,Zhonglong Zhang,Qiuchun Lu,Jiaqi Tang,Wenqiang Wu,Xun Han

Copper-based halides, a type of perovskite derivative, inherit their excellent optoelectronic properties and solution processability and also have the advantages of being nontoxic and stable. Despite the tremendous achievements of microfabrication in conventional halide perovskites, reports on copper-based halide array devices are rare due to their difficult high-quality crystallization. Here, by introducing single-crystal thin films grown by space confinement method as substrates, reliable photolithography based on their single crystals is successfully achieved and controllable homoepitaxial single-crystal arrays is demonstrated. By adjusting the substrate, angle, and growth time, the orientation, arrangement, and size of arrays could be controlled. Temperature and time are used to regulate the growth stage to obtain clean and appropriately sized arrays. ITO/Cs 3 Cu 2 I 5 /ITO neuromorphic device based on homoepitaxial arrays is developed. The variation of synaptic plasticity could be controlled by the number and frequency of light pulses. The device successfully simulated the process of “learning, forgetting, and relearning” in the human brain, demonstrating the potential of application in sensing-storage-computing-integrated devices.

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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2024 · IF 3.8

Free-Radical/Cationic Hybrid UV-Curable Silicone Resin for Age-Resistant Coatings

Shengjun Huang,Hong Huang,Xiaoxuan Liu,Hongping Xiang

To achieve the unique advantages of silicone resin and the free-radical/cationic hybrid UV-curing mechanism, a free-radical/cationic hybrid UV-curable silicone resin (MTQ-TQ-T) is synthesized from commercially available siloxanes, hexamethyldisiloxane (MM, M segment), phenyltrimethoxysilane (PTMS, T segment), γ-(2,3-epoxypropoxy)propyltrimethoxysilane (KH560, T segment), (3-methacryloxy)propyltrimethoxysilane (KH570, T segment), and tetraethyl orthosilicate (TEOS, Q segment). UV-curing kinetics indicates that the polymerization efficiency of MTQ-TQ-T initiated by free-radical and cationic dual photoinitiators is better than that of a single photoinitiator. As the molar ratio of cationic to free-radical photoinitiators (C/R) increases, the double-bond conversion first increases and then decreases, but the epoxy group conversion is the opposite. The optimal C/R and dose of dual photoinitiators are 1.5 and 10 wt %, respectively. After UV-curing, the coating has excellent overall performance including a gel content of 87.8%, a Shore A hardness of 85, a tensile strength of 4.23 MPa, and an impact strength of 5.48 kJ/m2. Its thermal decomposition temperature of 5 wt % is 338 °C, and the yellowing index only increases by 0.98 after thermal aging at 85 °C for 72 h. Moreover, UVMTQ-TQ1-T0.33 (the molar ratio, T/Q of 1 and KH560/570 of 0.33) shows good hydrophobicity with a contact angle of 87°, and it is still 89° after thermal aging. In addition, the adhesion of coating increases with the increase of epoxy groups, where UVMTQ-TQ1-T1 (the molar ratio, T/Q of 1 and KH560/570 of 1) has optimal adhesion with a shear strength and 180° peel strength of 1.7 and 0.9 MPa, respectively. Therefore, this free-radical/cationic hybrid UV-curable silicone resin will be used as aging-resistant coatings.

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JOURNAL OF WUHAN UNIVERSITY OF TECHNOLOGY-MATERIALS SCIENCE EDITION · 2024 ·Vol. 39 ·期 4 ·1053-1060 · IF 1.3

Fabrication and Properties of a New Reactive Diluent for Cationic UV Curing

Wu Zhengsen,Huang Biwu,Liu Yuansheng,Shen Han

The reactive diluent prepared by siloxane modified Trimethylene oxide can improve the performance of the UV curing system. Therefore, 1,7-bis [(3-ethyl-3-methoxyoxacylobutane) propyl] octadecylosiloxane (BEMOPOMTS) was synthesized from diethyl carbonate, trimethylopropanes, allyl bromide, and 1,1,3,3,5,5,7,7-octadecylosiloxane as the main raw materials. BEMOPOMTS can be used as reactive diluents in the field of cationic UV curing. It has good thermal stability, and the addition of BEMOPOMTS significantly improves the tensile strength and elongation at break of epoxy resin. Compared with the pure epoxy resin, adding 20% BEMOPOMTS increased the elastic modulus by 25% to 677 MPa.

CAS / MDL: 108-88-3
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CHEMICAL RESEARCH IN CHINESE UNIVERSITIES · 2024 ·Vol. 40 ·期 2 ·279-286 · IF 3.1

In-situ UV-Vis Spectroscopy of Trisulfur Radicals in Lithium-Sulfur Batteries

Dou Renju,Wang Qin,Ren Xiaoyan,Lu Lehui

Here we employ in-situ UV-Vis spectroscopy to monitor the sulfur redox reaction with oxygen-containing molecules as an additive, for example, biphenyl-4,4′-dicarboxylic acid (BDC). Furthermore, Raman spectrum, electron paramagnetic resonance (EPR), and electrospray ionization-mass spectrometry (ESI-MS) measurements reveal that the formation of BDC-S •‒ 3 complexes can establish the long-term stability of polysulfide radicals, change the kinetics of sulfur redox reaction, and then generate decent capacity retention and rate capability. According to the density functional theory (DFT) analysis, S •‒ 3 radicals are the underlying product of S 2‒ 6 cleavage, owing to the decreased chemical energy and the increased stability of S •‒ 3 radicals through Lewis acid-base interaction. The assembled Li-S batteries with BDC additive deliver a high reversible capacity of 420 mA·h·g −1 over 200 cycles with over 98% Coulombic efficiency, under the current density of 0.2 C.

CAS / MDL: 100-21-0
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Polymers · 2024 ·Vol. 16 ·期 11 ·1555 · IF 4.7

Improving Hemocompatibility of Polysulfone Membrane by UV-Assisted Grafting of Sulfonated Chitosan

Sheng Yan,Yunren Qiu

The most prevalent type of hemodialysis membrane is polysulfone (PSf). However, due to inadequate biocompatibility, it significantly compromises the safety of dialysis for patients. In this study, we modify the surface of the PSf membrane with 2,4-dihydroxybenzophenone (DBPh) groups to serve as anchoring sites during UV irradiation. Subsequently, a tailored sulfonated dihydroxy propyl chitosan (SDHPCS) is grafted onto the modified PSf membrane to compensate for the deficiencies in hydrophilic additives. The modified PSf membrane exhibits outstanding hydrophilicity and stability, as demonstrated by its characterization and evaluation. This paper focuses on investigating the interaction between platelet membrane formation, protein adsorption, and anticoagulant activity. The results show that the modified PSf membrane exhibits remarkable enhancement in surface hydrophilicity, leading to a significant reduction in protein and platelet adsorption as well as adhesion.

CAS / MDL: 131-56-6 7790-94-5
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2018 ·Vol. 25 ·期 11 ·10808-10819 · IF 2.8

UV modification of biochar for enhanced hexavalent chromium removal from aqueous solution

Peng Zhongya,Zhao Hang,Lyu Honghong,Wang Lan,Huang Hua,Nan Qiong,Tang Jingchun

This study was conducted to understand the effects of ultraviolet (UV) irradiation on the physicochemical properties and the hexavalent chromium (Cr(VI)) removal ability of biochar. Structural and morphological analysis showed that UV irradiation increased the specific surface area of biochar and added a large amount of oxygen-containing functional groups (e.g., carboxyl, lactonic, and hydroxyl) to biochar’s surface. Batch sorption experimental results showed that UV-modified biochar (UVBC) produced at the pyrolysis temperature of 300 °C, the irradiated time of 24 h, and the irradiation distance of 40 mm exhibited excellent Cr(VI) removal ability (from 1.11 mg/g for BC to 20.04 mg/g for UVBC, a 18.1-fold increase). The adsorption kinetics and adsorption isotherm data agreed well with the pseudo-second-order model and Freundlich model, respectively. Experimental and modeling results suggest that the oxygen-containing functional groups and specific surface areas of biochars were notably increased by UV irradiation, which enhanced Cr(VI) adsorption by surface complexation. X-ray photoelectron spectroscopy (XPS) analysis of UVBC before and after reaction with Cr(VI) showed that reduction occurred during Cr(VI) adsorption. The energy consumption of UV modification is 2.7 MJ per gram of UVBC produced, which is comparable to that in activated carbon. The results showed that the method of UV modification of biochar is a very novel and effective method for the adsorption of Cr(VI) in solution.

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SOLAR ENERGY MATERIALS AND SOLAR CELLS · 2010 · IF 3.858

UV irradiation-initiated MMA polymerization to prepare microcapsules containing phase change paraffin

Sude Ma,Guolin Song,Wei Li,Pengfei Fan,Guoyi Tang

Microencapsulated phase change material (MEPCM), paraffin, with polymethylmethacrylate shell was prepared by introducing UV irradiation to an O/W emulsion polymerization for approximately 30   min under constant stirring. The results of differential scanning calorimetry analyses indicate that the latent heat and the content of paraffin of microcapsules are 101   J   g −1 and 61.2   wt%, respectively. The phase transition temperature of MEPCM ranges from 24 to 33   °C. The MEPCM was characterized using scanning electron microscopy and Fourier transform infrared spectroscopy. Thermal gravimetric analysis results show that the MEPCM is degraded into two distinguishable steps. Accelerated thermal cycling tests also indicate that the MEPCM displays a good thermal reliability. Gypsum boards composed of as-prepared MEPCM show a good temperature-regulated property. Based on all these results, it can be concluded that the microencapsulated paraffin as MEPCMs have good potential for thermal energy storage purposes such as phase change material slurries, solar space heating applications, textiles and building materials .

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POLYMER BULLETIN · 2011 ·Vol. 68 ·期 3 ·729-743 · IF 1.215

Synthesis and properties of UV-curable hyperbranched polyurethane acrylate oligomers containing photoinitiator

Han Wensong,Lin Baoping,Zhou Yidan,Song Jiangang

The hyperbranched polyurethane acrylate oligomers containing photoinitiator were synthesized by modifying the second-generation hyperbranched poly(amine-ester) with isophorone diisocyanate-2-hydroxyethylacrylate and isophorone diisocyanate-2-hydroxy-2-methylpropiophenone at different feed ratio. The elemental analysis, FT-IR and NMR methods are used for structural characterization, molecular weights, and polydispersities, photosensitive groups and thermal properties of the oligomers were analyzed by gel permeation chromatography, UV–Vis spectra and thermogravimetric analysis, respectively. UV-curing properties were characterized by FT-IR at different curing time. In addition, the solubilities of the oligomers were also examined.

CAS / MDL: 818-61-1 4098-71-9
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

Three-in-one: Saturated, UV-protective and anti-bacterial structural colored textiles

Lan-Xing Gao,An Tang,Wei-Long Bi,Zhijie Zhu,Yu Tian

Structural color based textiles have attracted significant attention owing to their potential in facilitating environmentally-friendly and durable coloration processes. However, the improvement of color saturation in textiles based on structural color is still under continuous investigation. Additionally, there is a rising demand for textiles featuring specialized functionalities such as anti-bacteria and anti-ultraviolet properties in daily life. In this study, a “three-in-one” amorphous photonic structure (APS) and multi-functional textile design is performed to achieve high structural color saturation, UV protection, and anti-bacteria properties. In this system, poly(styrene-butyl acrylate-methacrylate) (P(St-BA-MAA)) colloidal particles are used as building blocks, black titanium dioxide (TiO 2 ) is used as black dopant , and water-soluble polyurethane (WPU) is used as the binder. The WPU demonstrates a significant capability to enhance the color fastness of APS/TiO 2 textiles. The strong absorption of incoherent scattered light by black TiO 2 in the visible range plays a crucial role in achieving a highly saturated APS-based textile. In addition, the doped black TiO 2 possesses strong UV–visible light absorption and anti-bacterial capabilities, thereby supporting the development of textiles functionalized with UV protection and anti-bacteria. Our proposed simplified approach to fabricating high color saturation and functionalized APS/TiO 2 textiles demonstrates significant potential for eco-textile coloring in line with market demands.

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