Protein and Polysaccharide-Based Fiber Materials Generated from Ionic Liquids: A Review

Protein and Polysaccharide-Based Fiber Materials Generated from Ionic Liquids: A Review

natural biomacromolecules such as structural proteins and polysaccharides composed of the basic building blocks of life: amino acids and carbohydrates. Understand their molecular structure, self-assembly and interaction in solvents such as ionic liquids (ILS) is very important to release new material flora, revolutionizing the way we make multi-structural systems and multi-functional with tunable physicochemical properties.

Ionic liquids are superior to organic solvents because they do not produce unwanted by-products and is considered a green replacement for their reusability. In addition, they will significantly improve the biopolymer miscibility with other materials while maintaining the mechanical properties of the biopolymer in the final product. Understanding and controlling the physicochemical properties of the biopolymer in an ionic liquid matrix will be very important for the progress leading to the ability to create powerful multi-level 1D structural fiber material.

It will also help to predict the relationship between fiber and protein secondary structure conformation or carbohydrate crystallinity, thereby creating potential applications for cell growth signaling, ionic conductivity, liquid diffusion and thermal conductivity, and some applications in the biomedical and environmental sciences. It will also enable the regeneration of the biopolymer composite fiber materials with useful functionality and a customized selection is important for additive manufacturing.

Specific skills fiber materials have proven to vary based on their fabrication methods including electrospinning and post-treatment. This review serves to provide basic knowledge is commonly used in protein and polysaccharide biopolymer and method of fabrication of their fiber from a variety of ionic liquids, as well as the effect of post-treatment on fiber materials and their applications in biomedical research and pharmaceuticals, wound healing, filter environmental and chemical research sustainable and green.

 Protein and Polysaccharide-Based Fiber Materials Generated from Ionic Liquids: A Review
Protein and Polysaccharide-Based Fiber Materials Generated from Ionic Liquids: A Review

Increased absorption of phenol solution using a modified silver nanoparticles Palm Kernel Shell Activated Carbon

Modified Palm Kernel Shell Activated Carbon (PKSAC) use silver nanoparticles (Ag-NP-PKSAC) investigated the uptake of phenol from aqueous solution. The effect of temperature (500-700 ° C), time (90-120 minutes), and alkali concentration (0.1-0.5 M) were studied on yield and methylene blue number for synthesis.

The influence of the initial concentration (100-200 mg / L), agitation (150-250 rpm), the contact time (30-120 minutes), and adsorbent dosage (0.15 to 0.25 g) were studied in batch experiments on the percentage elimination of phenol , MCC, char, PKSAC and Ag-NP-PKSAC characterized using BET, FTIR, SEM, and the proximate analysis. Synthesis PKSAC optimum at 608 ° C, 0.5 M KOH, and carbonization holding time of 60 minutes.

Canine Brucella IgM (Brucella-IgM) ELISA Kit

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EUR 124.8

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EUR 511.65

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Bovine Brucella Antibody IgM (Brucella-IgM) ELISA Kit

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Description: Human (Homo sapiens)

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KTE62702-5platesof96wells 5 plates of 96 wells
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Description: Quantitative sandwich ELISA for measuring Human Brucella Antibody IgM (Brucella-Ab-IgM) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.

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SL1598Ra - Ask for price

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AssayStar 384 Square Well Assay Plate, Black Solid Bottom - 100 plates

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  • Ask for price
  • Ask for price
  • Ask for price
  • 1 plate of 96 wells
  • 10 plates of 96 wells each
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96-well Black Polystyrene Plate

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96-well Black Polystyrene Plate

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Human Brucella-IgM ELISA Kit

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Protein A-coated ELISA plate (8 well strips, 96 wells/plate) 5 plates/pack

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2 x Clear 96 well Plate, 2EA

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5 x Clear 96 well Plate, 5EA

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2 x Clear 96 well Plate, 2EA

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4 x Clear 96 Well Plate, 4EA

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96 Deep Well Plate Round Wells - PK50

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3455 PK50
EUR 318.6

96 Well Roche Style PCR Plate

PCR1218 PK50
EUR 223.74

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EUR 261.9

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96 well filter plate (no filter)

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EUR 229.5

Black Half Area 96 Well Plate, 1EA

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EUR 313.16

96-well plate Plasmid DNA Prep (mini)

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96 Well PCR Plate Clear Wells - PK50

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EUR 290.25

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96-Well Plate Viral DNA Miniprep Kit

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EUR 495.86

96-Well Plate Plasmid DNA Miniprep Kit

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EUR 300.37

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EUR 186.19

Protein A&G-coated ELISA plate (8 well strips, 96 wells/plate) 5 plates/pack

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96-Well Plate DNA Cleanup Miniprep Kit

BS369 5XPlates, 480prep
EUR 300.37

96-Well Plate DNA Cleanup Miniprep Kit

BS3692 2xPlates, 192prep
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Phenol optimum absorption was 85.64, 90.29 and 91.70% for PKSAC, Ag-NP-PKSAC and commercial adsorbents, respectively. The mechanism of phenol adsorption followed Langmuir isotherm and best described as a physio-absorption by the pseudo-second-order kinetics. Phenol showed high affinity (ΔS ° = 0.0079 kJ / mol K) for Ag-NP-PKSAC with favorable adsorption (AG ° = -1.551 kJ / mol) at high temperature for the endothermic (ΔH ° = 1.072 kJ / mol) properties system. The results obtained in this study compares favorably with literature.

Sean

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