Upcycling of PVC waste to high-value sorbent with KOH-activation for efficient removal of organic dyes.

Polyvinyl chloride (PVC), known for its chemical stability and flame-retardant qualities, has many uses in various fields, such as pipes, electric wires, and cable insulation. Research has established its potential recovery as a fluidic fuel through pyrolysis, but the use of PVC pyrolysis oil, which is tainted by chlorine, is constrained by its low heat value and harmful environmental effects. This study engineered a layered double hydroxide (LDH) to tackle these challenges. The LDH facilitated dechlorination during PVC pyrolysis and bolstered thermal stability via cross-linking. During pyrolysis with LDH, PVC was transformed into carbon-rich precursors to sorbents. Chemical activation of these residues using KOH created sorbents with a specific surface area of 1495.4 m2 g⁻1, rendering them hydrophilic. These resulting sorbents displayed impressive adsorption capabilities, removing up to 486.79 mg g⁻1 of methylene blue and exhibiting the simultaneous removal of cations and anions.

Ultrafast and on-demand oil/water separation with vertically aligned cellulosic smart sponge.

Slow oil sorption speed of commercial non-woven polypropylene (PP) sorbent remains a major challenge for efficient clean-up of oil spillage. Adsorption-based polymeric sponge oil removing offers an appealing way to solve this challenge by increasing surface area. However, the tortuous oil sorption path and plastic waste after oil uptake are two long-standing bottlenecks for realizing efficient oil spill removal. Here, we report a vertically aligned-biomass fiber junctioned sorbents (a-BFJS), by confining delignified biomass with carbon nanotube (CNT), polyvinyl alcohol (PVA), and methyltrimethoxysilane (MTMS). The sorbent shows an excellent performance towards xylene sorption capacity with uptake about 50 g g-1 within 10 s. This is due to the wide and short pathway of their aligned channels, which improves the capillary effect and fast oil transport in the oriented channels. Moreover, the sponge exhibits fast oil sorption-desorption kinetics enabled by simple mechanical squeezing. We further engineered a scalable rapid continuous oil skimming with simple peristaltic pump. The oil recovering using a-BFJS realized high oil selectivity from xylene/water emulsion. Our demonstration of the high-performance aligned channel sorbent and scalable oil removing sponge offers an eco-friendly and promising strategy for efficiently removing oil from oil spills from water.

Polyolefin-based electrospun fibrous matrices embedded with magnetic nanoparticles for effective removal of viscous oils.

In this work, we present a poly (ethylene-co-1-octene)-based fibrous matrix prepared via electrospinning for highly efficient removal of viscous oils. The sorbent consisting of linear low density polyethylene (LLDPE) allows selective absorption of crude oil spills at the water surface without the need for additional isolation of the matrix prior to the refining process. Moreover, the high specific pore volume of the LLDPE sorbent with uniform fibrous morphology was shown to enable the sorbent reach 81.5 ± 5.9% of its equilibrium absorption capacity within 5 min. Furthermore, magnetic nanoparticles (MNP) are incorporated into each fiber comprising the matrix to facilitate the recovery process via external magnetic field without altering the intrinsic absorption capacity. We envision that these sorbents offer a sustainable route for the quick and thorough clean-up of spilled oil due to their high absorption capacity, fast absorption rate, ease of recovery, and absence of secondary waste.

Electrospinning fabrication of magnetic nanoparticles-embedded polycaprolactone (PCL) sorbent with enhanced sorption capacity and recovery speed for spilled oil removal.

The use of oil-soaked sorbents in the recovery and cleaning of oil spills presents challenges due to disposal. Recently, magnetic nanoparticle (MNP) based collection has been gaining interest as a new technique to lower the amount of labor required to treat oil spills. In this study, we devised a new method for the preparation of a magnetic nanoparticle (MNP) embedded polycaprolactone (PCL) sorbent with oleophilic and environmentally friendly features, capable of bring easily collected under a magnetic field. Compared with conventional polypropylene sorbents, the MNP embedded PCL sorbent (MNP/PCL) displayed excellent Arabian light (AL) crude oil sorption capacity (45.7 g g-1) and decreased the absorption time of the oil-soaked sorbent due to its electrospun structure and efficient distribution of hydrophobic MNPs. Furthermore, the MNP/PCL based sorbent became fully pyrolyzed under certain temperatures and conditions. The MNP embedded PCL-based sorbent demonstrated broad applicability and utility in large scale oil spill projects.

Superhydrophobic polypropylene sorbent derived from discarded face masks: A highly efficient adsorbent for oil spill sorbent.

Globally, an estimated 130 billion face masks are used and disposed of every month. Thus, recycling or upcycling discarded face masks has attracted significant attention due to economic benefits and environmental concerns. To reduce the amount of used face masks going to waste, this study features a superhydrophobic face mask prepared by simple chemical modification with environmentally preferable alkane solvents (n-hexane, n-heptane, and n-decane), that is effective as a sorbent for oil spill cleanup. All alkanes examined increased the surface roughness of the face masks and improved face mask hydrophobicity. The heptane treated face mask (at 90 °C for 1 h), can adsorbed Arabian light crude oil up to 21 times of their weight on the water surface. In addition, chloroform, toluene, gasoline, and diesel were adsorbed 18, 13, 8 and 16 times, respectively. More importantly, heptane has a high recycling efficiency as a treatment solvent and is reusable for at least 10 cycles of mask surface treatment. Consequently, this inexpensive and easily fabricated material is a promising development in waste face mask (WFM) upcycling.

Highly efficient and recyclable polyolefin-based magnetic sorbent for oils and organic solvents spill cleanup.

The oil dispersants have been applied in a broad oil pollution area, but the dispersed oil caused environmental problems during sedimentation. Unlike oil dispersants, flake type polyolefin-based oil absorbent (PA) is not emulsified and shows excellent swelling characteristic for oil removal. However, the sprayed PA flakes cannot be fully collected due to its tiny architectures, the uncollected flakes can cause unintentional secondary pollution. In this study, we develop a kind of flake type polyolefin-based magnetic absorbent (PMA) hybridized with magnetic nanoparticle, to facilitate the collection process. The magnetic nanoparticle is uniformly dispersed in PMA due to the hydrophobic functionalization of iron oxide nanoparticle. This enables the convenient collection of isolated sorbent flakes even when they were placed in the marine system and show a desirable oil recovery performance up to about 37 times for organic solvent. Moreover, oil-soaked PMA flakes can be fully converted into refined oil via a pyrolysis process. After pyrolysis, the thermally undecomposed compounds, which comprise of carbon residue and magnetic nanoparticle, can be also separated by a magnet. The as-prepared flake type PMA possesses good oil recovery performance, fast magnetic response, and efficient oil recycling, thus representing an environmentally promising method for oil spill cleanup.

Recent advances in the development of nitric oxide-releasing biomaterials and their application potentials in chronic wound healing.

Chronic wounds, such as pressure ulcers, vascular ulcers and diabetic foot ulcers (DFUs), often stay in a state of pathological inflammation and suffer from persistent infection, excess inflammation, and hypoxia, thus they are difficult to be healed. Nitric oxide (NO) plays a critical role in the regulation of various wound healing processes, including inflammatory response, cell proliferation, collagen formation, antimicrobial action and angiogenesis. The important role of NO in wound healing attracts intensive research focus on NO-based wound healing therapy. However, the application of NO gas therapy needs to resolve the intrinsic shortcomings of gas therapy, such as short storage and release times as well as temporal and spatial uncontrollability of the release mode. So far, various types of NO donors, including organic nitrates (RONO2), nitrites (RONO), S-nitrosothiols (RSNOs), nitrosamines, N-diazeniumdiolates (NONOates), and metal-NO complexes, have been developed to solidify gaseous NO and they were further encapsulated in or conjugated onto a variety of biomaterial vectors to develop NO delivery systems. NO synthetic enzyme mimics to catalyze the production and release of NO from L-arginine have also been developed. This paper reviews recent advances of NO donors, biomaterial vectors, thus-formed NO delivery systems, as well as recently emerged NO synthetic enzyme mimics. Furthermore, this review also summarizes the functions of NO releasing biomaterials that would benefit chronic wound healing, including antibacterial properties and the promotion of angiogenesis, as well as the convenient combination of light/thermal induced NO release with light/thermal therapies, and the prospects for future developing trends in this area.

Aqueous Two-Phase System (ATPS)-Based Polymersomes for Particle Isolation and Separation.

Aqueous two-phase systems (ATPSs) have been widely used in the separation, purification, and enrichment of biomolecules for their excellent biocompatibility. While ultracentrifugation and microfluidic devices have been combined with ATPS to facilitate the separation of biomolecules and achieve high recovery yields, they often lack the ability to effectively isolate and separate biomolecules in low concentrations. In this work, we present a strategy that leverages the preferential partitioning of biomolecules in ATPS droplets to efficiently separate model extracellular vesicle (EV) particles. We demonstrate that the additional oil phase between the inner ATPS droplets and the aqueous continuous phase in triple emulsion droplets resolves the size controllability and instability issues of ATPS droplets, enabling the production of highly monodisperse ATPS-based polymersomes with enhanced stability for effective isolation of ATPS droplets from the surrounding environment. Furthermore, we achieve separation of model EV particles in a single dextran (DEX)-rich droplet by the massive production of ATPS-based polymersomes and osmotic-pressure-induced rupture of the selected polymersome in a hypertonic solution composed of poly(ethylene glycol) (PEG).

Water and Oil Insoluble PEGDA-Based Microcapsule: Biocompatible and Multicomponent Encapsulation.

Despite the recent development in various materials capable of encapsulating biomolecules, there exist limited reports on multicomponent encapsulation in biocompatible microcapsules. In this letter, we utilize the molecular weight dependent solubility of poly(ethylene glycol) diacrylate (PEGDA) and droplet microfluidics to achieve direct encapsulation of both hydrophilic and hydrophobic cargoes in PEG microcapsules. By using PEGDA 250 as the middle phase, we demonstrate that these PEGDA-based microcapsules allow simultaneous encapsulation of both hydrophilic and hydrophobic cargoes. We further confirm the validity of this approach by demonstrating that complex biomolecule such as protein can be effectively encapsulated within these PEGDA-based microcapsules.

Improved ATR-FTIR detection of hydrocarbons in water with semi-crystalline polyolefin coatings on ATR elements.

In situ measurement of hydrocarbons in water is critical for assuring the safety and quality of drinking water and in environmental remediation activities such as the cleanup of oil spills. Thus, effective detection methods of hydrocarbons in aqueous environments are important and several methods have been used for this type of sensing, including spectroscopic techniques, fiber optic sensors, and chromatography. However, under aqueous conditions, small amounts of hydrocarbons are difficult to detect due to their low concentration in water and robust sensing of these types of compounds in an aqueous environment remains a challenging analytical task. Hydrophobic polymer coatings have been widely used to concentrate hydrocarbons for attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) detection at the surface of an ATR crystal by preventing water molecules from penetrating into the polymer coating while absorbing hydrocarbons. However, in typical coating designs only thin films (<5 µm) can be applied onto the ATR sensor due to the decrease in detection limit and sensitivity to hydrocarbons with increasing film thickness. This paper demonstrates that a semi-crystalline linear low-density polyethylene (LLDPE) polymer coating with thicker thickness (40 µm) can be applied effectively for in situ ATR-FTIR detection of hydrocarbons in aqueous solution. The ATR signal is enhanced by the polymer coating which swells in response to the hydrocarbons and prevents water accumulation at the IR detection interface. Coating the ATR element with a LLDPE film (crystallinity = 12%) reduced the detection time for various hydrocarbons, including toluene, benzene and chloroform. The detection limits and kinetics of the ATR-FTIR detection were not significantly altered when the thickness of the LLDPE coating was increased to improve its mechanical properties which represents a significant improvement from coatings published in the literature. The LLDPE coating described in this research has the potential to be applied as a sensor coating for rapid detection of hydrocarbon-based substances or non-polar biomolecules in aqueous environments.

Polyolefin-based interpenetrating polymer network absorbent for crude oil entrapment and recovery in aqueous system.

In this research, a series of different two polyolefin-based interlaced polymer network material was prepared with a semi-crystalline linear low density polyethylene (LLDPE, thermoplastic) and a crosslinked 1-decene/divinylbenzene (1-D/DVB, elastomer) having high crude oil absorption capacity. The prepared absorbents, LLDPE/D/DVB, were characterized by NMR, TEM, contact angle measurement and TGA analysis. It was observed that the mixing ratio of two interlaced polymer network played a crucial role in determining its crude oil absorption capacity. The swelling capacity of absorbent prepared from a 1:1 mixing of LLDPE and D/DVB (0.2 ml) exhibit high removal efficiency in crude oil absorption over 40 g/g at both 25 °C and 0 °C. The removal of the absorbed crude oil from the water surface is effective. As the absorbent made of polyolefin materials have pure hydrocarbon content, offer significant advantages such as high absorption capacity, simple recovery, and recyclability.

An Ionophore-Based Anion-Selective Optode Printed on Cellulose Paper.

A general anion-sensing platform is reported based on a portable and cost-effective ion-selective optode and a smartphone detector equipped with a color analysis app. In contrast to traditional anion-selective optodes using a hydrophobic polymer and/or plasticizer to dissolve hydrophobic sensing elements, the new optode relies on hydrophilic cellulose paper. The anion ionophore and a lipophilic pH indicator are inkjet-printed and adsorbed on paper and form a "dry" hydrophobic sensing layer. Porous cellulose sheets also allow the sensing site to be modified with dried buffer that prevents any sample pH dependence of the observed color change. A highly selective fluoride optode using an AlIII -porphyrin ionophore is examined as an initial example of this new anion sensing platform for measurements of fluoride levels in drinking water samples. Apart from Lewis acid-base recognition, hydrogen bonding recognition is also compatible with this sensing platform.

Increased Hydrogel Swelling Induced by Absorption of Small Molecules.

The water and small molecule uptake behavior of amphiphilic diacrylate terminated poly(dimethylsiloxane) (PDMSDA)/poly(ethylene glycol diacrylate) (PEGDA) cross-linked hydrogels were studied using attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy. These hydrogel networks absorbed more water as the PEGDA content of the network increased. In contrast to typical osmotic deswelling behavior that occurs when liquid water equilibrated hydrogels are immersed in small molecule solutions with water activities less than unity, water-swollen gels immersed in 2-acrylamido-2-methylpropanesulfonic acid (AMPS-H) solutions rapidly regained their water content within 4 min following an initial deswelling response. In situ ATR-FTIR analysis of the hydrogel film during the dynamic swelling experiment indicated that small molecule absorption into the gel played an important role in inducing gel reswelling in low water activity solutions. This aspect of polymer gel water uptake and interaction with small molecules is important for optimizing hydrogel coatings and hydrophilic polymer applications where there is an interaction between the internal chemical structure of the gel and electrolytes or other molecules in solution.

Characterization of Polyethylene-Graft-Sulfonated Polyarylsulfone Proton Exchange Membranes for Direct Methanol Fuel Cell Applications.

This paper examines polymer film morphology and several important properties of polyethylene-graft-sulfonated polyarylene ether sulfone (PE-g-s-PAES) proton exchange membranes (PEMs) for direct methanol fuel cell applications. Due to the extreme surface energy differences between a semi-crystalline and hydrophobic PE backbone and several amorphous and hydrophilic s-PAES side chains, the PE-g-s-PAES membrane self-assembles into a unique morphology, with many proton conductive s-PAES channels embedded in the stable and tough PE matrix and a thin hydrophobic PE layer spontaneously formed on the membrane surfaces. In the bulk, these membranes show good mechanical properties (tensile strength >30 MPa, Young's modulus >1400 MPa) and low water swelling (λ < 15) even with high IEC >3 mmol/g in the s-PAES domains. On the surface, the thin hydrophobic and semi-crystalline PE layer shows some unusual barrier (protective) properties. In addition to exhibiting higher through-plane conductivity (up to 160 mS/cm) than in-plane conductivity, the PE surface layer minimizes methanol cross-over from anode to cathode with reduced fuel loss, and stops the HO• and HO2• radicals, originally formed at the anode, entering into PEM matrix. Evidently, the thin PE surface layer provides a highly desirable protecting layer for PEMs to reduce fuel loss and increase chemical stability. Overall, the newly developed PE-g-s-PAES membranes offer a desirable set of PEM properties, including conductivity, selectivity, mechanical strength, stability, and cost-effectiveness for direct methanol fuel cell applications.

Ladder-type SAW filters using thinned density of randomly distributed "hot" electrodes.

A new method for the design of relatively narrowband ladder-type SAW filters is proposed. It consists of the thinning procedure and consecutive randomization of positions of the remaining transductive periods inside the IDT to suppress undesirable additional passbands. A 0.9% fractional bandwidth filter on LiTaO(3) 42°-cut was designed and manufactured using the proposed approach.

Fragile histidine triad gene alterations are not essential for hepatocellular carcinoma development in South Korea.

AIM: To establish the role of FHIT in the pathogenesis hepatocellular carcinoma (HCC). METHODS: We examined genomic alterations, as well as, mRNA and protein expression patterns from the FHIT gene, in 48 surgically resected hepatocellular carcinoma (HCC) tissues. Additionally, p53 mutations were analyzed. RESULTS: Aberrant FHIT transcripts were detected in 11 of 48 surrounding non-tumor liver tissues and 27 of 48 HCC samples (22.9% vs 56.3%, P = 0.002). No point mutations were identified within the open reading frame region of FHIT. Loss of heterozygosity (LOH) of the FHIT locus was detected in 4 of 42 informative cases for D3S1300, and 3 of 29 informative cases for D3S1313. Reduced expression of FHIT protein (Fhit) was observed in 8 (16.7%) of 48 HCC samples, with complete loss of Fhit in only 1 case. There were no associations with abnormal transcripts, LOH, and Fhit expression. p53 mutations were identified in 9 of the 48 HCC cases. However, none of the cases displayed a G to T transversion at p53 codon 249. CONCLUSION: Aberrant FHIT transcripts were more common in HCC tissues as compared to non-cancerous liver tissues. However, Fhit expression was lost or reduced in a minor fraction of HCC tissues, while it was strongly expressed in non-cancerous liver tissues. Therefore, our study suggests that FHIT plays a role in relatively few HCC cases in South Korea.

Low incidence of hepatic artery thrombosis after pediatric liver transplantation without the use of intraoperative microscope or parenteral anticoagulation.

The risk of hepatic artery thrombosis (HAT) after pediatric liver transplantation (PLT) has been reported to range from 0 to 25%. We report our experience focusing on the interrelationships between risk factors, surgical technique and the incidence of HAT after liver transplantation in the pediatric age group. From February 18, 1997 to December 31, 2003, 150 consecutive liver transplants were performed in 132 pediatric patients. There were similar numbers of whole grafts when compared with partial grafts, 80 (53.3%) vs. 70 (46.7%), p = 0.30. Four grafts (2.7%) developed HAT. Of the grafts with HAT, three were successfully revascularized within the first 24 h. Only one graft (0.66%) was lost to HAT. A single surgeon utilizing 3.5-6.0 magnification loupes performed all but one hepatic arterial anastomoses. All patients were followed postoperatively by a daily ultrasound protocol and with anticoagulation of aspirin and alprostadil only. Living and deceased donor left lateral segment grafts had an increased rate of HAT when compared with whole liver grafts. HAT with subsequent graft loss may be minimized in PLT with the use of surgical loupes only, anticoagulation utilizing aspirin, alprostadil, and daily ultrasounds.