scholarly journals Solution Blowing Spinning Technology towards Green Development of Urea Sensor Nanofibers Immobilized with Hydrazone Probe

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 531
Author(s):  
Mohamed H. El-Newehy ◽  
Hany El-Hamshary ◽  
Waheed M. Salem
Keyword(s):  
Cellulose Acetate ◽  
Calcium Alginate ◽  
Limit Of Detection ◽  
Cellulose Nanofibers ◽  
Molecular Probe ◽  
Homogeneous Distribution ◽  
Sem Images ◽  
Film Sensor ◽  
Solution Blowing ◽  
Urease Enzyme

Cellulose has been one of the most widespread materials due to its renewability, excellent mechanical properties, biodegradability, high absorption ability, biocompatibility and cheapness. Novel, simple and green colorimetric fibrous film sensor was developed by immobilization of urease enzyme (U) and tricyanofuran hydrazone (TCFH) molecular probe onto cellulose nanofibers (CNF). Cellulose acetate nanofibers (CANF) were firstly prepared from cellulose acetate using the simple, green and low cost solution blowing spinning technology. The produced CANF was exposed to deacetylation to introduce CNF, which was then treated with a mixture of TCFH and urease enzyme to introduce CNF-TCFH-U nanofibrous biosensor. CNF were reinforced with tricyanofuran hyrazone molecular probe and urease enzyme was encapsulated into calcium alginate biopolymer to establish a biocomposite film. This CNF-TCFH-U naked-eye sensor can be applied as a disposable urea detector. CNF demonstrated a large surface area and was utilized as a carrier for TCFH, which is the spectroscopic probe and urease is a catalyst. The biochromic CNF-TCFH-U nanofibrous biosensor responds to an aqueous medium of urea via a visible color signal changing from off-white to dark pink. The morphology of the generated CNF and CNF-TCFH-U nanofibrous films were characterized by different analytical tools, including energy-dispersive X-ray patterns (EDX), polarizing optical microscope (POM), Fourier-transform infrared spectroscopy (FT-IR) and scanning electron microscope (SEM). SEM images of CNF-TCFH-U nanofibers demonstrated diameters between 800 nm and 2.5 μm forming a nonwoven fabric with a homogeneous distribution of TCFH/urease-containing calcium alginate nanoparticles on the surface of CNF. The morphology of the cross-linked calcium alginate nanoparticles was also explored using transmission electron microscopy (TEM) to indicate an average diameter of 56–66 nm. The photophysical performance of the prepared CNF-TCFH-U was also studied by CIE Lab coloration parameters. The nanofibrous film biosensor displayed a relatively rapid response time (5–10 min) and a limit of detection as low as 200 ppm and as high as 1400 ppm. Tricyanofuran hydrazone is a pH-responsive disperse dye comprising a hydrazone detection group. Determination of urea occurs through a proton transfer from the hydrazone group to the generated ammonia from the reaction of urea with urease.

Isolation of Cellulose Nanofibers (CNFs) based on Ball-milling Technique Combined with Supercritical Carbon dioxide/ethanol Pretreatment

2021 ◽  
Author(s):  
Zhijun Hu ◽  
Xinyu Cao ◽  
Guanhong Huang ◽  
Daliang Guo
Keyword(s):  
Thermal Stability ◽  
Reaction Time ◽  
Ball Milling ◽  
High Efficiency ◽  
Cellulose Nanofibers ◽  
Sem Images ◽  
Tempo Oxidation ◽  
Good Thermal Stability ◽  
Ethanol Pretreatment ◽  
Ball Milling Technique

Abstract Here, a new pretreatment method has been developed to produce CNFs from micro-fibrillated cellulose (MFC) by supercritical CO 2 pretreatment followed with ball-milling (SCB). MFC was obtained from cotton stalk by chemical purification.Experimental factors were controlled to enhance the properties of SCB-CNF, meanwhile a comparative study was conducted with the method of TEMPO oxidation and microfluid homogenization (TMH). Compared to TMH-CNF, the SCB-CNF has such advantages as Energy saving, high efficiency and environmental protection, indicating a wide application in heat-resistant materials, load materials and other fields. The solid yields of P-MFC after supercritical CO 2 pretreatment gradually decreased together with the temperature and the reaction time. Scanning electron microscope (SEM) images of the SCB-CNF and TMH-CNF show that the morphology of the SCB-CNF was basically acicular but that of the TMH-CNF was mainly soft fibrous. The SCB-CNF is smaller in width and shorter in length, and its size is between CNC and CNF. Thermal gravimetric results suggest that the thermal stability of the SCB-CNF was substantially higher than those of the TMH-CNF. XRD results indicate that the crystallinity showed an initial increasing trend and then declined with increasing temperature and reaction time, and the crystallinity value of SCB-CNF was larger than that of CNFs. The smaller SCB-CNF became rougher and had a larger surface area. High crystallinity make good thermal stability, short and coarse fiber, easier to disperse than CNF, less energy consumption for dispersion, better than 3D mesh. It can be widely used in polymer composites, reinforcing agents, membrane materials and other fields.

Influence of Ambient Temperature and Light-curing Moment on Polymerization Shrinkage and Strength of Resin Composite Cements

2018 ◽  
Vol 43 (6) ◽  
pp. 619-630 ◽  
Author(s):  
N Rohr ◽  
JA Müller ◽  
J Fischer
Keyword(s):  
Tensile Strength ◽  
Resin Composite ◽  
Indirect Tensile Strength ◽  
Homogeneous Distribution ◽  
Sem Images ◽  
Polymerization Shrinkage ◽  
Ambient Temperatures ◽  
Light Curing ◽  
Indirect Tensile ◽  
Composite Cements

ABSTRACT Objective: The purpose of this study was to establish a clinically appropriate light-curing moment for resin composite cements while achieving the highest indirect tensile strength and lowest polymerization shrinkage. Methods and Materials: Polymerization shrinkage of seven resin composite cements (Multilink Automix, Multilink Speed Cem, RelyX Ultimate, RelyX Unicem 2 Automix, Panavia V5, Panavia SA plus, VITA Adiva F-Cem) was measured at ambient temperatures of 23°C and 37°C. Testing was done for autopolymerized and light-cured specimens after light application at either 1, 5, or 10 minutes after mixing. Indirect tensile strength of all cements was measured after 24 hours of storage at temperatures of 23°C and 37°C, for autopolymerized and light-cured specimens after light application 1, 5, or 10 minutes after mixing. To illustrate filler size and microstructures, SEM images of all cements were captured. Statistical analysis was performed with one-way ANOVA followed by post hoc Fisher LSD test (α=0.05). Results: Final polymerization shrinkage of the resin composite cements ranged from 3.2% to 7.0%. An increase in temperature from 23°C to 37°C as well as the light-curing moment resulted in material dependent effects on the polymerization shrinkage and indirect tensile strength of the cements. Polymerization shrinkage of the cements did not correlate with the indirect tensile strength of the cement in the respective groups. Highest indirect tensile strengths were observed for the materials containing a homogeneous distribution of fillers with a size of about 1 μm (Multilink Automix, Panavia V5, VITA Adiva F-Cem). Conclusion: The magnitude of the effect of light-curing moment and temperature increase on polymerization shrinkage and indirect tensile strength of resin composite cements is material dependent and cannot be generalized.

scholarly journals Development of Pd/TiO2 Porous Layers by Pulsed Laser Deposition for Surface Acoustic Wave H2 Gas Sensor

Nanomaterials ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 760 ◽  
Author(s):  
Izabela Constantinoiu ◽  
Cristian Viespe
Keyword(s):  
Acoustic Wave ◽  
Frequency Shift ◽  
Pulsed Laser Deposition ◽  
Surface Acoustic Wave ◽  
Limit Of Detection ◽  
Pulsed Laser ◽  
Laser Deposition ◽  
High Porosity ◽  
Porous Films ◽  
Sem Images

The influence of sensitive porous films obtained by pulsed laser deposition (PLD) on the response of surface acoustic wave (SAW) sensors on hydrogen at room temperature (RT) was studied. Monolayer films of TiO2 and bilayer films of Pd/TiO2 were deposited on the quartz substrates of SAW sensors. By varying the oxygen and argon pressure in the PLD deposition chamber, different morphologies of the sensitive films were obtained, which were analyzed based on scanning electron microscopy (SEM) images. SAW sensors were realized with different porosity degrees, and these were tested at different hydrogen concentrations. It has been confirmed that the high porosity of the film and the bilayer structure leads to a higher frequency shift and allow the possibility to make tests at lower concentrations. Thus, the best sensor, Pd-1500/TiO2-600, with the deposition pressure of 600 mTorr for TiO2 and 1500 mTorr for Pd, had a frequency shift of 1.8 kHz at 2% hydrogen concentration, a sensitivity of 0.10 Hz/ppm and a limit of detection (LOD) of 1210 ppm. SAW sensors based on such porous films allow the detection of hydrogen but also of other gases at RT, and by PLD method such sensitive porous and nanostructured films can be easily developed.

scholarly journals Microfabricated Au-Film Sensors for the Voltammetric Determination of Hg(II)

Proceedings ◽  
2018 ◽  
Vol 2 (13) ◽  
pp. 1518
Author(s):  
Maria Tsetsoni ◽  
Eleni Roditi ◽  
Christos Kokkinos ◽  
Anastasios Economou
Keyword(s):  
Electrode Surface ◽  
Limit Of Detection ◽  
Anodic Stripping Voltammetry ◽  
Stripping Voltammetry ◽  
Voltammetric Determination ◽  
Film Sensor ◽  
Au Film ◽  
Working Electrode ◽  
Anodic Stripping

In this work, a microfabricated Au-film sensor was designed and fabricated for thevoltammmetric determination of Hg(II). The electrode was fabricated on a silicon chip with astandard microengineering approach utilizing photolithography for patterning the electrode shapeand sputtering for deposition of thin Cr and Au films on the surface of the sensors. The sensorswere used for the determination of trace Hg(II) with anodic stripping voltammetry (ASV): initiallyHg(II) in the sample was accumulated on the Au working electrode surface by reduction andformation of an Au(Hg) amalgam followed by oxidation of the preconcentrated metallic Hg using asquare wave voltammetric scan. The limit of detection was 1.5μgL−1 and the coefficient of variationof 10 consecutive measurements was 3.1%.

scholarly journals Preconcentration of morphine in urine sample using a green and solvent-free microextraction method

2019 ◽  
Vol 8 (1) ◽  
pp. 542-550
Author(s):  
Bamdad Riahi-Zanjani ◽  
Mahdi Balali-Mood ◽  
Zarrin Es’haghi ◽  
Ahmad Asoodeh ◽  
Adel Ghorani-Azam
Keyword(s):  
Urine Sample ◽  
Small Volume ◽  
Limit Of Detection ◽  
Solid Phase ◽  
Medical Toxicology ◽  
Significant Loss ◽  
Solvent Free ◽  
Environmental Damage ◽  
Limit Of Quantification ◽  
Sem Images

Abstract The ability of extraction and preconcentration of small amounts of substances from biological samples is very important in medical toxicology. On the other hand, minimal use of organic solvents is an important issue to prevent environmental damage. In the present study, we developed a new solid phase microextraction fiber using plant extracts as sorbent for extraction and preconcentration of morphine in urine sample. For this purpose, raw carbon nanotubes (CNTs) were functionalized with tobacco extracts. Functionalization was confirmed by Fourier transform infrared (FTIR) and Raman spectroscopy in addition to scanning electron microscope (SEM) images. The functionalized CNTs were coated on polypropylene hollow fiber. The results of HPLC analysis showed that the produced fiber could preconcentrate a very low concentration of morphine (0.25 ng/ml) in small volume of urine samples. Limit of detection (LOD) and limit of quantification (LOQ) for the produced fiber were determined 0.25 ng/ml and 0.825 ng/ml, respectively, and recovery of the fiber was determined 89% at LOQ. The produced fiber provided a recyclable and solvent free method for extraction of a trace amount of morphine, which can be successfully used for up to 30 times with no significant loss in the extraction efficiency.

scholarly journals Synthesis and Characterization of a High Flux Nanocellulose–Cellulose Acetate Nanocomposite Membrane

Membranes ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 70 ◽  
Author(s):  
Nancy Li ◽  
Jackie Zheng ◽  
Pejman Hadi ◽  
Mengying Yang ◽  
Xiangyu Huang ◽  
...  
Keyword(s):  
Polymer Matrix ◽  
Energy Requirement ◽  
Cellulose Nanofibers ◽  
Membrane Resistance ◽  
High Energy ◽  
Sem Images ◽  
Membrane Performance ◽  
Aspect Ratios ◽  
Membrane Flux

Despite the advantages of membrane processes, their high energy requirement remains a major challenge. Fabrication of nanocomposite membranes by incorporating various nanomaterials in the polymer matrix has shown promise for enhancing membrane flux. In this study, we embed functionalized cellulose nanofibers (CNFs) with high aspect ratios in the polymer matrix to create hydrophilic nanochannels that reduce membrane resistance and facilitate the facile transport of water molecules through the membrane. The results showed that the incorporation of 0.1 wt % CNF into the polymer matrix did not change the membrane flux (~15 L · m − 2 · h − 1 ) and Bovine Serum Albumin (BSA) Fraction V rejection, while increasing the CNF content to 0.3 wt % significantly enhanced the flux by seven times to ~100 L · m − 2 · h − 1 , but the rejection was decreased to 60–70%. Such a change in membrane performance was due to the formation of hydrophilic nanochannels by the incorporation of CNF (corroborated by the SEM images), decreasing the membrane resistance, and thus enhancing the flux. When the concentration of the CNF in the membrane matrix was further increased to 0.6 wt %, no further increase in the membrane flux was observed, however, the BSA rejection was found to increase to 85%. Such an increase in the rejection was related to the electrostatic repulsion between the negatively-charged CNF-loaded nanochannels and the BSA, as demonstrated by zeta potential measurements. SEM images showed the bridging effect of the CNF in the nanochannels with high CNF contents.

scholarly journals Optimization and Application of Electrochemical Transducer for Detection of Specific Oligonucleotide Sequence for Mycobacterium tuberculosis

Biosensors ◽  
2018 ◽  
Vol 8 (3) ◽  
pp. 84 ◽  
Author(s):  
Ricardo Corrêa ◽  
Filipe da Cruz ◽  
Cátia Santos ◽  
Thiago Pimenta ◽  
Diego Franco ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Mycobacterium Tuberculosis ◽  
Limit Of Detection ◽  
Polymeric Film ◽  
Adsorption Parameters ◽  
Limit Of Quantification ◽  
Sem Images ◽  
Complementary Oligonucleotide ◽  
Scan Rate ◽  
Oligonucleotide Sequence

In this study, the electropolymerization of 4-hydroxyphenylacetic acid (4-HPA) over graphite electrodes (GE) was optimized, aiming its application as a functionalized electrochemical platform for oligonucleotides immobilization. It was investigated for the number of potential cycles and the scan rate influence on the monomer electropolymerization by using cyclic voltammetry technique. It was observed that the polymeric film showed a redox response in the region of +0.53/+0.38 V and the increase in the number of cycles produces more electroactive platforms because of the better electrode coverage. On the other hand, the decrease of scan rate produces more electroactive platforms because of the occurrence of more organized coupling. Scanning electron microscopy (SEM) images showed that the number of potential cycles influences the coverage and morphology of the electrodeposited polymeric film. However, the images also showed that at different scan rates a more organized material was produced. The influence of these optimized polymerization parameters was evaluated both in the immobilization of specific oligonucleotides and in the detection of hybridization with complementary target. Poly(4-HPA)/GE platform has shown efficient and sensitive for oligonucleotides immobilization, as well as for a hybridization event with the complementary oligonucleotide in all investigated cases. The electrode was modified with 100 cycles at 75 mV/s presented the best responses in function of the amplitude at the monitored peak current values for the Methylene Blue and Ethidium Bromide intercalators. The construction of the genosensor to detect a specific oligonucleotide sequence for the Mycobacterium tuberculosis bacillus confirmed the results regarding the poly(4-HPA)/GE platform efficiency since it showed excellent sensitivity. The limit of detection and the limit of quantification was found to be 0.56 (±0.05) μM and 8.6 (±0.7) μM, respectively operating with very low solution volumes (15 µL of probe and 10 µL target). The biosensor development was possible with optimization of the probe adsorption parameters and target hybridization, which led to an improvement in the decrease of the Methylene Blue (MB) reduction signal from 14% to 34%. In addition, interference studies showed that the genosensor has satisfactory selectivity since the hybridization with a non-specific probe resulted in a signal decrease (46% lower) when compared to the specific target.

scholarly journals Recyclable SERS-Based Immunoassay Guided by Photocatalytic Performance of Fe3O4@TiO2@Au Nanocomposites

Biosensors ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 25 ◽  
Author(s):  
Yuanyuan Du ◽  
Hongmei Liu ◽  
Yiran Tian ◽  
Chenjie Gu ◽  
Ziqi Zhao ◽  
...  
Keyword(s):  
Photocatalytic Performance ◽  
Limit Of Detection ◽  
Specific Antigen ◽  
High Sensitivity ◽  
Shell Nanoparticles ◽  
Sem Images ◽  
Potential Measurement ◽  
Surface Enhanced Raman ◽  
Clinical Measurements ◽  
Core Shell Nanoparticles

A novel recyclable surface-enhanced Raman scattering (SERS)-based immunoassay was demonstrated and exhibited extremely high sensitivity toward prostate specific antigen (PSA). The immunoassay, which possessed a sandwich structure, was constructed of multifunctional Fe3O4@TiO2@Au nanocomposites as immune probe and Ag-coated sandpaper as immune substrate. First, by adjusting the density of outside Au seeds on Fe3O4@TiO2 core-shell nanoparticles (NPs), the structure-dependent SERS and photocatalytic performance of the samples was explored by monitoring and degradating 4-mercaptobenzonic acid (4MBA). Afterwards, the SERS enhancement capability of Ag-coated sandpaper with different meshes was investigated, and a limit of detection (LOD), as low as 0.014 mM, was achieved by utilizing the substrate. Subsequently, the recyclable feasibility of PSA detection was approved by zeta potential measurement, absorption spectra, and SEM images and, particularly, more than 80% of SERS intensity still existed after even six cycles of immunoassay. The ultralow LOD of the recyclable immunoassay was finally calculated to be 1.871 pg/mL. Therefore, the recyclable SERS-based immunoassay exhibits good application prospects for diagnosis of cancer in clinical measurements.

scholarly journals Removal of Copper from Water by Adsorption with Calcium-Alginate/Spent-Coffee-Grounds Composite Beads

Materials ◽  
2019 ◽  
Vol 12 (3) ◽  
pp. 395 ◽  
Author(s):  
Roberto Torres-Caban ◽  
Carmen Vega-Olivencia ◽  
Luis Alamo-Nole ◽  
Daisy Morales-Irizarry ◽  
Felix Roman-Velazquez ◽  
...  
Keyword(s):  
Calcium Alginate ◽  
Alginate Beads ◽  
Order Kinetic ◽  
Spent Coffee Grounds ◽  
Sem Images ◽  
Composite Beads ◽  
Coffee Grounds ◽  
Initial Ph ◽  
Equilibrium Data ◽  
Experimental Values

Calcium Alginate/Spent-Coffee-Grounds composite beads (CA-SCGs beads), which were made of two different proportions of alginate and spent-coffee-grounds (3:3 and 3:10), respectively, were used to adsorb Cu2+ in aqueous solution. These beads were compared with calcium alginate beads (CA beads) and spent-coffee-grounds (SCGs) in terms of adsorption capacity and rate of adsorption. The experiments were carried out at an initial pH of 4 at 30 °C with initial concentrations of Cu2+ from 10 ppm to 100 ppm. Equilibrium data was fitted with Langmuir, Freundlich and Sips models, and a pseudo-second-order kinetic equation. The Sips model showed the best correlation with the experimental values. CA-SCGs (3:3) beads showed a faster adsorption rate versus the CA beads. Also, CA-SCGs (3:3) beads showed a larger capacity of adsorption according to the Sips model, but not in the Langmuir model. FT-IR spectra and SEM images were taken for characterization. This study has shown that the CA-SCGs (3:3) beads have a synergistic effect, combining the capacity of adsorption of CA beads with the kinetics of the SCGs. The CA-SCGs beads have proven to be an effective adsorbent of Cu2+. Therefore, they can provide a use for the SCGs; which are considered pollutants in landfills.

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