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Natural Fibers - Science topic

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I like to know how seawater we use in cement mixing and maybe some about using plastic, glass, and natural fibers.
Thank you,
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The ratio of mixing cement with seawater depends on the type of concrete being made and the required properties. However, it is generally not recommended to use seawater for mixing concrete due to its high chloride content, which can lead to corrosion of reinforcement steel and affect the long-term durability of the structure.
Typical Mixing Ratio for Cement Using Seawater
If seawater must be used due to availability issues, the typical mix ratio is similar to normal concrete but with additional considerations for durability:
  1. Standard Mix Ratio (by weight):Cement : Sand : Aggregate : Water Common ratios: 1:2:4 or 1:1.5:3 Water-cement ratio (W/C) = 0.45 - 0.6 (adjusted based on workability)
  2. Seawater Considerations:Use sulfate-resistant cement (Type V) to minimize sulfate attack. Limit seawater usage to unreinforced concrete to avoid steel corrosion. Consider adding pozzolanic materials (e.g., fly ash, silica fume) to reduce permeability. Use corrosion-resistant reinforcements (e.g., epoxy-coated, stainless steel, or fiber-reinforced polymer bars).
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Natural fiber, Polymer
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I would suggest searching publications around the topic, and then contacting the group involved in those publications. Normally, sending an email to the group leader or director showing interest is a good first step.
The other option would be to look for the opportunity in different webpages. Regarding this, I recently found a LinkedIn post with different websites you can check:
Best of luck in your research!
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If natural fibre micron size increase, what about the thermal conductivity of polymer composite material. pls explain the mechanism behind that.
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Volume fraction of fibre and matrix is nothing but the cross sectional areal fractions. Assume your composite specimen has a cross section of 20mm width and 10mm thickness. Cross sectional area is 200mm2. If the fibre occupies 120mm2 and the matrix 80mm2, then the fibre areal/volume fraction is 120/200=0.6 or 60%. Balance matrix/polymer is 40%.
Thermal Conductivity of Composite = VF of Fibre x Thermal Conductivity of Fibre + VF of Matrix x Thermal Conductivity of Matrix.
TC of Composite = 0.6 x TC of Fibre + 0.4 x TC of Matrix.
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I am excited to tell you that I am the Guest Editor of a new Special Collection titled: 'Advanced Bio-Composite Development through the Valorization of Agricultural Waste.' This is being published by Sage Publishing in their journal "Composites and Advanced Materials," which is a JCR-ranked, peer-reviewed, open-access journal. Here is a link to the journal: "https://lnkd.in/dJzXs8Nk
". I launched this unique collection because synthetic fiber-reinforced composites (FRCs) have significantly increased in various applications. This rise in usage has raised concerns about environmental and sustainability issues due to the energy-intensive and unsustainable production processes involved in fabricating these composites. Limited recyclability and disposal options for FRCs have led to a growing demand for biocomposites made from natural fibers, such as agricultural waste, combined with biodegradable polymers to replace FRCs. Natural fiber-based biocomposites offer several advantages over traditional composites, including increased sustainability, strength, and durability. Additionally, many agricultural wastes remain underutilized and could be explored to develop advanced biocomposites using various techniques. These techniques include utilizing natural fibers as reinforcement, filler, or a hybrid of both in the composite material. One of the main benefits of using agricultural waste in advanced biocomposites is that it reduces waste going to landfills and incinerators. Moreover, it helps minimize the environmental impact of manufacturing traditional composites, which often rely on synthetic fossil-fuel fibers. Please consider publishing your latest research in this Special Collection. If you are interested, don't hesitate to contact me with your suggested title, and I will pass on your details to Sage so they may work with you toward publication. As per Open Access publication requirements, you would be charged the total publication fee; however, the benefit is that your paper would appear not only in the regular issue but also in the Special Collections, thus attracting increased readership. Ongoing promotions for the Special Collection will ensure your paper continually receives views, downloads, and citations. Please feel free to contact me if you have any questions. I am excited to hear from you. I appreciate your consideration. Time is running out, so send your manuscript today!!!
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Thank you for sharing the opportunity to contribute to the Special Collection titled "Advanced Bio-Composite Development through the Valorization of Agricultural Waste" in the journal Composites and Advanced Materials by Sage Publishing. This initiative aligns with the growing interest in sustainable materials and the utilization of agricultural waste in composite development.
Composites and Advanced Materials is a peer-reviewed, open-access journal that welcomes submissions of original research articles, reviews, and short communications contributing to the science and engineering of composites and advanced materials.
SAGE Publishing
For researchers working on agrowaste valorization and biocomposites, this Special Collection offers a platform to showcase innovative work in transforming agricultural residues into valuable composite materials.
Submission Guidelines:
  • Manuscript Preparation: Ensure your manuscript adheres to the journal's formatting and style guidelines.
  • Online Submission: Submit your manuscript through the journal's online submission system.
  • Open Access Fees: Be aware of any article processing charges associated with open-access publication.
For detailed information on submission procedures and deadlines, please refer to the journal's official website.
SAGE Publishing
This Special Collection represents a significant opportunity to contribute to the advancement of sustainable materials science and the effective utilization of agricultural waste in composite material development.
Invitation to Join Dailyplanet.Club:
I would also like to invite you to join Dailyplanet.Club, a platform dedicated to fostering collaboration among researchers and innovators in fields such as biocomposites and sustainable development.
Benefits of Joining:
  • Networking Opportunities: Connect with experts and peers in your area of research.
  • Resource Sharing: Access a wealth of information and collaborative tools.
  • Support for Innovation: Engage in projects aimed at advancing sustainable technologies.
Membership is £5 per year, supporting the platform's mission to build a global community focused on innovation and sustainability. Visit Dailyplanet.Club to join and explore its offerings.
Looking forward to your participation!
Best regards,
James Henderson Mitchell
CEO, MJ HSA Ltd
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There is no ASTM standard or this. I don't want to prepare composite laminate and conduct shear test or IFSS. I want to make a decision in the treatment stage itself. Is it possible to embed one end of the natural fiber in a small piece of epoxy matrix and conduct a tensile test wherein fiber is pulled out of the matrix and force is noted ? Did someone try it out and got reliable results ? If there is no ASTM standard, then what is the way to go ?
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Embedding one end of a natural fiber in an epoxy matrix for a tensile test to assess fiber pull-out strength is a feasible and previously explored method, despite lacking an ASTM standard. This approach can yield reliable insights into fiber-matrix interactions without requiring composite laminates.
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Is there a fundamental theory of polymer fibers and nanofibers?
I work with polymer fibers and I am interested in whether there is a fundamental theory to describe them. Suppose fibers are composed of an amorphous rather than crystalline polymer. If they are very thin, they will be unstable for two reasons. Firstly, they have a large free surface area and hence high surface energy. Secondly they are usually composed of highly oriented polymer molecules, which are entropy depleted and tend to adopt a Gaussian coil conformation. Despite the effect of these two factors, nanofibers made of amorphous polymers can be stable in some cases.
Are there theories that estimate the limits of their stability (taking into account the flexibility of polymers and the interaction energy between links)? Are such theories applicable to partially crystalline polymers? I am 100% sure that these theories exist, could you please help me to find them?
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Dear Dmitry Bagrov, please have a look at the following book and the attached file. My Regards
Xiangwu Zhang
Fundamentals of Fiber Science
ISBN-13: 978-1605951195, ISBN-10: 9781605951195
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While the effects of growth, harvest, and supply conditions on natural fiber quality are
generally known, there is a lack of comprehensive studies that systematically examine how
these parameters impact the performance of natural fibers in composite materials. The
optimization of these conditions for specific fiber types, with the goal of enhancing their
effectiveness in composites, is not well documented in a unified manner.
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Optimizing the quality of natural fiber composites involves enhancing growth, harvesting, and supply chain parameters, as these factors significantly impact fiber properties. While individual effects are recognized, comprehensive studies examining their combined influence on composite performance are lacking. Future research should focus on developing integrated best practices to improve the effectiveness of specific natural fibers in composite applications.
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As far as my understanding goes, the intention of alkali treatment is to remove non-cellulosic hemicellulose, lignin, wax and other impurities and enhance the surface roughness and crystallinity. The molecular chains of cellulose rearrange themselves into closely packed long chain, thereby increasing the crystallinity. When non-cellulosic components that seal the gap between the microfibrils are removed the surface roughness increase.
However, when non-cellulosic components like hemicellulose and wax are removed, that exposes more hydrophilic cellulose to water. Also, lignin is hydrophobic, when it is removed all we have a hydrophilic cellulose.
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You asked the question and answered it yourself. Since the fibers are hydrophilic, they interact better with water, water spreads better along the fibers. They are better wetted by water. They interact better with a hydrophilic matrix. To interact with a hydrophobic matrix, they must be hydrophobized. Copper nanoparticles are well distributed in them.
Biocidal cotton material with copper nanoparticles was prepared by treating cloth surface with copper hydroxide in ammonia solution and by coagulation of surface gel and evening of the fiber surface followed by reduction of copper complexes to the atoms and nanoparticles.
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I do know the name of analytical methods, but not the method in detail. Kurschner and Hoffer’s method for cellulose determination. Klason method to determine lignin. Wax content by conrad method. Ash content was analyzed as per the ASTM E1755-61 standard.
I would like to know the method. Are there any references that you know ? and where such tests can be done in India, preferably South India. Are there any such laboratories ?
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The Kürschner and Hoffer method determines cellulose content by treating samples with nitric acid, while the Klason method quantifies lignin through sulfuric acid hydrolysis. The Conrad method assesses wax content via extraction processes, and ash content is analyzed according to ASTM E1755-61 standards.
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Is there a single JCPDS card for natural fiber ? My understanding is that all natural fibers basically have the same constituents albeit they are in different concentration. Cellulose, hemicellulose, lignin, pectin and wax. Natural fiber is a semi-crystalline material, so expect amorphous and crystalline indicators in the XRD graph.
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Natural fibers primarily consist of alpha-cellulose. The cellulose phase potentially alters based on treatments or processing conditions. The specific type of cellulose can be verified using the JCPDS file. This file is accessible for download via the accompanying software of the XRD machine. Within this software, JCPDS cards relating to all types of cellulose is available for manual comparison or automatic identification. The system handler can assist in extracting the JCPDS cards based on their licensing agreement.
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I know of a place in Tamil Nadu where for one sample cost is 5000. I am looking for a cheaper alternative.
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It is available in Coimbatore. I presume that you might be aware of it Muralishwara Kakunje
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This is the XRD plot of natural fiber. Usually in almost all the papers, 2 peaks appear for natural fiber. One broader amorphous peak at lower diffraction angle and lower intensity and another sharper crystalline peak at higher diffraction angle and higher intensity. Percentage crystallinity equation is PC = Intensity of crystalline peak/(intensity of crystalline + amorphous peaks). In my graphs I am getting multiple sharp peaks. Why is this ? Should I add up all the peak intensities to get total intensity of crystalline phase ?
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Gerhard Martens when exactly will you really call a peak crystalline ? What is the minimum width of the band that is needed to qualify as amorphous ? or is it subjective and must be complemented with other tests ?
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Would you please let me to know about the methods for measurement of medullation and Kemp % on animal? My problem is that the wool sampling and sending to laboratory is not possible. So I would like to verify the possibility of a method to measure Kemp/medullation % in wool rapidly on the animal. I know "Benzene test" (attached file) for distinguishing of Kemp fibers, but Benzene is a risky material. Furthermore the use of portable OFDA in our situation is not possible.
Is there safe substance similar to benzene that has the similar optical refractive index ? Which safe liquid can be found that has a light refractive index similar to wool? (1.54). Sincerely,
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Response to my question by CHATGPT:
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How we can measure Kemp % in wool without using of benzene?
ChatGPT
Measuring the Kemp percentage in wool typically involves microscopic examination, but it can be done without the use of benzene. Here's a general procedure using a microscope and without the use of benzene:
Materials Needed:
  1. Microscope: A microscope with sufficient magnification for detailed fiber examination.
  2. Prepared Wool Samples: Obtain representative wool samples for analysis.
  3. Slides and Coverslips: To prepare slides for microscopic examination.
  4. Light Source: Ensure proper lighting for clear visibility.
Procedure:
  1. Prepare Wool Samples:
    • Cut a small section of wool from the sample for analysis.
  2. Create Microscopic Slides:
    • Place a small amount of the wool sample on a microscope slide.
    • Add a coverslip to create a flat surface for examination.
  3. Microscopic Examination:
    • Examine the wool fibers under the microscope at sufficient magnification (typically 100x to 400x).
    • Identify kemp fibers, which are coarser, thicker, and often have a more translucent appearance compared to regular wool fibers.
  4. Count Kemp Fibers:
    • Count the number of kemp fibers in the sample.
    • For a more accurate measurement, consider counting kemp fibers in multiple fields of view and taking an average.
  5. Calculate Kemp Percentage:
    • Calculate the Kemp percentage using the formula:
Kemp Percentage=(Number of Kemp FibersTotal Number of Fibers)×100Kemp Percentage=(Total Number of FibersNumber of Kemp Fibers​)×100
Notes:
  • Quality of Microscope: Ensure that the microscope used provides clear and detailed visibility to distinguish between regular wool fibers and kemp fibers.
  • Sampling: For representative results, take multiple samples from different areas of the wool lot.
  • Observation Criteria: Define clear criteria for identifying kemp fibers to maintain consistency in your observations.
This method doesn't involve the use of benzene, but it's important to note that microscopic examination is still crucial. If you encounter challenges or limitations, you may want to explore advanced image analysis techniques or consider seeking assistance from a specialized laboratory equipped for fiber analysis. Always prioritize safety and ethical considerations in any testing procedures.
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But I need a quick and tool-free method without a microscope.
ChatGPT
I understand the need for a quick and tool-free method without a microscope. While a thorough analysis of Kemp fibers typically requires microscopic examination, you can try a more rudimentary visual inspection approach. Keep in mind that this method may not be as precise as microscopic examination but can provide a rough estimate. Here's a simplified method:
Visual Inspection Method:
  1. Prepare the Wool Sample:
    • Cut a small representative section of wool from your sample.
  2. Separation of Fibers:
    • Spread out the wool fibers and separate them as much as possible.
  3. Visual Inspection:
    • Examine the wool fibers visually for any noticeable differences.
    • Look for fibers that appear thicker, coarser, or have a more translucent quality compared to the majority of fibers.
  4. Count Kemp Fibers:
    • Count the number of fibers that exhibit characteristics of kemp fibers.
    • For a more accurate estimate, consider counting kemp fibers in multiple sections of the sample.
  5. Calculate Kemp Percentage:
    • Use the formula:
Kemp Percentage=(Number of Kemp FibersTotal Number of Fibers)×100Kemp Percentage=(Total Number of FibersNumber of Kemp Fibers​)×100
Considerations:
  • This method relies on visual inspection and is subject to individual judgment.
  • It provides a rough estimate and may not be as accurate as microscopic examination.
  • For a more precise measurement, consider sending samples to a laboratory equipped for detailed fiber analysis.
While this method does not involve a microscope or chemicals, it's important to note its limitations. For more accurate and reliable results, especially in commercial or research contexts, microscopic examination or professional laboratory analysis is recommended.
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Please explain this method with a photo
ChatGPT
I'm afraid I cannot provide images directly, but I can guide you on what to look for during a visual inspection for Kemp fibers. Please note that this method is a simplified approach and might not be as accurate as microscopic examination. For more precise analysis, consulting a professional laboratory is recommended.
Visual Inspection Steps:
  1. Prepare the Wool Sample:
    • Cut a small, representative section of wool from your sample.
  2. Separation of Fibers:
    • Spread out the wool fibers on a clean surface and separate them as much as possible.
  3. Visual Inspection:
    • Look for fibers that exhibit characteristics of Kemp fibers. Key features to observe include:
      • Thickness: Kemp fibers are often thicker and coarser than regular wool fibers.
      • Translucency: Kemp fibers may appear more translucent than regular wool fibers.
      • Color: Kemp fibers might have a different color or shading compared to the rest of the wool.
  4. Count Kemp Fibers:
    • Count the number of fibers that display these characteristics.
  5. Calculate Kemp Percentage:
    • Use the formula: Kemp Percentage=(Number of Kemp FibersTotal Number of Fibers)×100Kemp Percentage=(Total Number of FibersNumber of Kemp Fibers​)×100
Visual Reference (Not an Actual Photo):
In the visual reference above (not an actual photo), you can imagine identifying thicker and coarser fibers with a more translucent appearance as potential Kemp fibers.
Remember, this visual inspection method is a basic approach and may not capture all Kemp fibers. For more accurate results, especially for commercial or research purposes, microscopic examination or professional laboratory analysis is recommended.
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Please explain this method with a photo. Or find an internet link with a photo please.
ChatGPT
I'm unable to provide images directly or browse the internet for specific photos. However, I can guide you on what to look for during a visual inspection for Kemp fibers, and you can use a search engine to find images as references.
Visual Inspection for Kemp Fibers:
  1. Thickness and Coarseness:
    • Kemp fibers are often thicker and coarser than regular wool fibers. Look for fibers with a visibly larger diameter.
  2. Translucency:
    • Kemp fibers may appear more translucent or have a lighter color than regular wool fibers. Hold them up to the light to observe any differences in transparency.
  3. Color Variation:
    • Kemp fibers might have a different color or shading compared to the rest of the wool. Look for fibers with noticeable color differences.
  4. Comparative Analysis:
    • Place a regular wool fiber next to a potential Kemp fiber for a side-by-side comparison. This can help highlight any differences in thickness, translucency, or color.
To find images for reference, you can use a search engine and look for terms such as "Kemp fibers in wool" or "Kemp wool vs regular wool." Ensure that the sources are reputable or from educational institutions, as accurate identification may require expertise.
Remember, while visual inspection can provide a rough estimate, microscopic examination remains the gold standard for precise analysis. If you have concerns about the accuracy of your visual inspection, consider seeking professional assistance from a laboratory equipped for fiber analysis.
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Journal of natural fibers seems to have come down to Q2.
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Muralishwara Kakunje The following journals cover materials science and engineering, including natural fibers, with a broad scope, including Advanced Materials, Science Advances, Nano Letters, ACS Applied Materials, Polymer Composites, Green Chemistry, Biomacromolecules, and Materials Today.
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Please. Could someone propose to me a simple or detailed lab procedure to perform grafting copolymerization onto natural fibers?
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this article help you for graft copolymerization onto natural fibers
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I created a composite using natural fiber and polyester resin, natural fiber +epoxy resin.
I got stress-strain curve from tensile test.
what is the strain range for composite material finding the young modulus of the curve?
Epoxy ?
Polyester?
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Dear Suganth,
The composite products are designed generally to work in the strain range of 0.1% to 0.3%. Hence the young's modulus is the difference in stress in the 0.1% to 0.3% strain range divided by 0.002 strain.
What are the fibre and the matrix in your composite specimen?
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Should I get certain 'fungi' or buy enzymes and use it directly for biological treatment ? Which enzymes can be used ? Where to buy from ?
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W.J. Colonna My natural fiber is Pineapple Leaf Fiber. I need to remove lignin and other waxy substances from the surface of the fiber to enhance its interfacial adhesion with epoxy matrix and also to make it hydrophobic.
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In characterization of composites, why failure mechanism at microscopic level has not been investigated on natural fiber reinforced polymer composites?
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Necessity is the mother of invention. Any study will need resource, effort and time!
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Much research has been done with natural fibers. Is it possible to use natural resins to make a composite plate?
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Thank you for sharing this research.
You can have a look on lignin-based and covalent adaptable networks here.
Kind regards,
Davide
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For example. Coir or coconut husk fibers are short. How can make a continuous fiber out of it. Idea is to prepare unidirectional continuous coir fiber polymer composite.
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The process of converting short natural fibers, such as coir or coconut husk fibers, into continuous strands is known as spinning. Spinning involves twisting the short fibers together to create a continuous yarn or thread. This can be done using a variety of techniques, including hand spinning, drop spinning, and using a spinning wheel.
In the case of coir fibers, the process typically involves first soaking the fibers in water to soften them and make them more pliable. The fibers are then carded or combed to align them and remove any impurities. Once the fibers are prepared, they can be spun into a continuous yarn using one of the spinning techniques mentioned above.
Once the coir fibers have been spun into a continuous yarn, they can be used to create a unidirectional continuous coir fiber polymer composite. This involves combining the coir yarn with a polymer matrix to create a composite material with improved strength and durability.
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Banana fiber mat is treated with 4% NaOH in distilled water - 4-hour immersion
Banana fiber mat length is reduced from 30cm to 21 cm. How to avoid shrinkage?
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In some cases for fabrics, we work under tension;
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Hello,
I hope this serious message "call for collaboration" could successfully reach the right professors and/ or funders, both in academic and industrial fields, who are really interested in the research area of "Biomass of Natural Fibers" and thier beneficial effect on a diversity of industrial engineering applications.
Recently, I was deeply involved in the mentioned research area and I have a particular contribution in a project closely related to that mentioned in the above title. To be comprehensive, I’m really willing to lead a research team or join a brilliant team by working under a leadership supervision of one of the esteemed professors in the mentioned research field. I will be so honered to transfer my experience earned from my latest successful project, and I’m sure that an aimful idea for establishing such a researching team work could be a very good step towards a prosperous future in making a multidesciplined progress in this research area and for opening many rooms for academics and indusrtial researchers who are interested in this field to have a prosperous future in thier career in line with the strategic sustainability development taking place worldwide and specifically in countries that are classified to be on popularized with thier agricultural development.
I’m willing to hear inspiring news and welcoming to any questions and feedback from all people who are interested in the idea by any way.
Best wishes,
Faithfully
Eyad Khalaf
PhD in Chemical Engineering, Polymer Composites
Agricultural Wastes Recycling & Sustainability
Tel.no.: +201001488248
Cairo, Egypt
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Dear Professor,
Below is a related article.
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Is there any method available commercially?
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Use a Universal cutter machine.
Please refer to the below article.
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Is micro-strain (ε= β/4tan θ) and Dislocation Density (δ=1/D^2) applicable to natural fiber urea formaldehyde composites as well as inoc,nano and metallic materials? if yes, then can anyone share research paper on it's my findings of those parameters are δ=3.708807 and ε=4.384302.
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Dear friend Dimple Bishnoi
Yes, micro-strain and dislocation density can be calculated from XRD data files of natural fiber urea formaldehyde composites as well as inorganic, nano and metallic materials. The microstrain is defined as the root mean square of variations in the lattice parameters across the sample. The dislocation density is defined as the number of dislocations per unit volume (What is the best method to determine.....).
I couldn't find a research paper that matches your findings of δ=3.708807 and ε=4.384302. However, I found a research paper that discusses the calculation of microstrain and dislocation density from XRD data files (What is the best method to determine.........). You may find it helpful.
I hope this helps!
Source:
(3) Approximation of crystallite size and microstrain via XRD line .... https://www.sciencedirect.com/science/article/abs/pii/S0042207X11003745.
(4) strain and dislocation density from XRD data - 14 - YouTube. https://www.youtube.com/watch?v=aWJ_m4Y0ZtE.
(5) X‐Ray Diffraction Microstrain Analysis for Extraction of Threading .... https://onlinelibrary.wiley.com/doi/10.1002/pssb.201900579.
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Do the -OH groups of natural fibers interact (other than hydrogen bond) with the diisocyanate (MDI) into a natural fiber-reinforced polyurethane (polyol and diisocyanate) composite?
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Yes it reacts with diisocyanate like a chemical treatment of fiber.
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One researcher did ballistic performance of kevlar fiber impregnated with nanosilica/ polyethylene glycol shear thickening fluid. And he loaded 10, 15, 20Wt% of Nanosilica with polyethylene glycol.
After fabrication, how we can confirm the equal distribution of nanosilica over the kevlar. Whether nanosilica is spread all over the kevlar equally or not?
How I can confirm? Any SEM, TEM test required ?
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You can use SEM/EDS to check for homogeneity of Si distribution. If you expect non homogeneity on 1-100 micron scale, you may want to use line scans of Si radiation (maps are not as sencitive). If scale is in range of millimeters or cantimeters, you may want to perform spot analisis for a lot of spots or use not a micro analytical technique, like XRD.
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I am looking for development of natural fiber based epoxy composite. If the selected natural fiber will be less porous than consumption of epoxy will be less and developed composite will be light weight
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As intrinsic fiber porosity is essentially linked to the Lumen of natural fibers, I suggest you research existing data on "Lumen diameter" of your prospective raw fibers. Might also want to check "Coarseness" of the fibers, as it will impact their stiffness.
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Why do micro-cracks forms in the matrix zones of FRP composites?
(a) Is it a Defect ?
(b) Does it has any effect on the initiation of fracture during the load applied?
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Micro-cracks can form in the matrix zones of fiber reinforced polymer (FRP) composites for a variety of reasons. Some potential causes of micro-cracking in FRP composites include:
  1. Residual stresses: FRP composites can be subject to residual stresses that are induced during the manufacturing process, such as those caused by curing or cooling. These residual stresses can cause micro-cracking in the matrix zones.
  2. Environmental factors: Exposure to environmental factors such as temperature fluctuations, moisture, and UV radiation can cause micro-cracking in the matrix zones of FRP composites.
  3. Load-induced cracking: The applied load can cause micro-cracking in the matrix zones of FRP composites, particularly when the load is applied at a high rate or when the composite is subjected to cyclic loading.
Micro-cracking in the matrix zones of FRP composites may be considered a defect, depending on the specific context and the severity of the cracks. In general, micro-cracking can affect the mechanical properties of the composite, such as its strength and stiffness, and may also affect its durability and service life.
Micro-cracks can also play a role in the initiation of fracture during the applied load. In general, micro-cracks can act as sites of stress concentration, and may promote the propagation of larger cracks when the composite is subjected to further loading. This can ultimately lead to failure of the composite material.
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I am following ASTM D7264 for conducting Flexural strength test of natural fiber polymer composite. Initially support span to thickness ratio of 32:1 was planned but due to miscommunication 32:1 is now total length to thickness ratio. Now if I am using 20:1 which is also allowed as per the ASTM standard I will have 36% of total length as overhanging portion. The standard recommends about 20%, doesn't say if it os minimum or maximum. Does taking higher overhanging length effect the result?
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The standard does recommend that the overhanging length should be about 20% of the total length, but it does not specify a minimum or maximum value. However, it is possible that a higher overhanging length could affect the results of the test.
In general, a longer overhanging length may result in a higher bending moment at the point of maximum load, which could lead to higher flexural strength values. However, it is also possible that a longer overhanging length could result in additional bending deformation or failure at the outermost fibers, which could lead to lower flexural strength values.
Therefore, it is important to consider the effect of the overhanging length on the results of the test and to carefully follow the recommended guidelines in the standard. It may also be helpful to conduct additional tests with different overhanging lengths to understand how this parameter affects the flexural strength of the composite material.
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Chemical treatment is done to ensure better fiber-polymer bonding by diminishing water absorbing tendency of natural fibers. Good mechanical properties are expected after this operation. Nevertheless, is it possible to have lower tensile, flexural properties in composites than the untreated ones? If so, what could be the possible reasons behind?
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It is possible that chemical treatment of natural fibers could affect the mechanical properties of fiber reinforced polymer composites. There are several factors that can influence the impact of chemical treatment on the mechanical properties of the composite, including the type of chemical used, the concentration of the chemical, the duration of the treatment, and the properties of the fibers and matrix material.
For example, some chemical treatments may cause the fibers to become more brittle, which could lead to a decrease in the tensile and flexural strength of the composite. Other treatments may cause the fibers to become more hydrophilic, which could lead to an increase in the moisture uptake of the composite and a decrease in its mechanical properties.
It is important to carefully consider the potential impacts of chemical treatment on the mechanical properties of the composite and to conduct appropriate testing to confirm the effects of the treatment. It may also be necessary to optimize the chemical treatment conditions in order to achieve the desired properties in the composite.
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I want to know the process and characterization techniques to extract cellulose nano crystal from natural fibers..
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I have got FTIR spectra of natural fibers and would like to know the surface concentration of lignin and cellulose. Is there any method for quantitative calculation for different components based on FTIR? How?
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bit of confusion as you try to figure out some quantitative info from basically a qualitative datasheet, you can try a passive way, firstly get a FTIR of non-modified fiber, and then compare the intensity of the desired functional group of your modified fiber.
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I have conducted 5 % concentrated alkaline (NaOH) treatment for my woven natural fiber (HEMP) to remove the impurities and unwanted wax that present in the fiber. To my surprise, after the chemical treatment hemp fiber colour changed as well as diameter of the fiber bundle got increased more than 50 %. Can anyone tell me the reason?
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Thank you for your valuable suggestions Vadym Chibrikov and Pierre Caulet sir. i will go through the article that u have referred...
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I need to test tensile properties of woven bidirectionally woven fiber which will be used to prepare composites. How do I measure the tensile properties (tensile strength and modulus) of it ? There is a standard for tear strength D5587 − 15 that measures tear strength of partially torn fabric. But this cannot be related to tensile strength since tensile strength is actually stress that can be handled to resist yield or fracture (MPa). Tear strength is actually force needed to completely tear a already torn fabric. So, please let me know the suitable standard to measure tensile strength.
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ASTM D3039. It's preferred to test the sample in both warp and weft directions but in the interest of time and to save the sample cost, you can test in only one direction (in the case of plain weave only) as you will get the same results.
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I would like to perform surface roughness of natural fibers by either using AFM or Laser micrsocpy, what are the main sample preparation steps involved for better results and accurate measurement?
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Hello
I would suggest that you measure your natural fibers using a microscope with calibrated scale bars, so you could have roughly ideas how big features of your fibers are. If the feature is small enough i.e. less than 10nm. You can try to use AFM.
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specimen will develop from hybrid natural fibers
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Dear Mohamed Mohamed, theoritically speaking, it is the same since mass and volume are interelated, but for practical reasons and to reduce errors, weighting a solid mass is more easy and convinient than to take its volume. My Regards
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I have found mostly the modulus of elasticity gradually increases with fiber percentage. If it is a must, then why does it happen? Is the reverse of it, I mean, gradually decrement of modulus possible?
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Dear Monishita Deb, not only fiber content but there are other additional deciding parameters, such as the fibers' dimensions and orientation, tight interface and so on. When the elastic modulus increases, it means that the matrix is becoming progressively resisting deformation, and this in turn means that the major stress input is well supported and transmitted by the reinforcing fibers. Please have a look at the following documents. My Regards
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if you can send the link of related papers?
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Thank you @ Vijayan dharanendran and @ Ramasamy Siva sir for your responses.
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Usually, we use tensile strength and youngs modulus to determine the properties of natural fibers. Why don't we use specific strength and specific modulus?
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Dear,
Please kindly refer below articles.
Article Lignocellulosic fiber reinforced composites: Progress, perfo...
Article A Comprehensive Review of Techniques for Natural Fibers as R...
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What are the risks of moisture absorption in the natural fibers exposed by drilling?
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I need Pineapple leaf fiber to fabricate composite material for research purpose. Where can I buy it from ?
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Extraction is best option. Chemical extraction method using NaOH will save time.
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The weaved fiber I have is plain weaved bi-directional natural fiber. I need find its tensile strength. The ASTM standard D3039 applicable to PMCs is not applicable to weaved fibers, fiber mats, etc. D5587 − 15 trapezoidal method of determining tear strength applies to most fabrics including woven fabrics, air bag fabrics, blankets, napped fabrics, knitted fabrics, layered fabrics, pile, and nonwoven fabrics. Am I technically correct in using this standard ? Have anyone used this standard before ? Please share your experience.
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How do I find chemical composition of natural fiber. Since cellulose, hemicellulose are all organic containing C, H and O elementally, how to find the chemical composition not elemental which can be determined from SEM-EDX.
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Pierre Caulet I need to prove that the incoming raw material from the supplier is the one I ordered. I ordered for Pineapple Leaf Fiber. So, right now I have decided to conduct FTIR analysis which qualitatively proved it. But it doesn't give the quantitative information on how much alpha-cellulose, hemicellulose and lignin the fiber contains.
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I am working on natural fiber epoxy composites. The Poissons ratio of composite can be calculated theoretically based on composites rule. But, what are the experimental techniques to evaluate the composites Poisson's ratio? Poisson's ratio of fiber and matrix is known.
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Hello,
In this case, the material is assumed to be orthotropic. Thus, you should conduct tension test in three directions and to use strain gauges to measure the deformation in the three direction. Then use the formula as Fares Mohammed Laid Rekbi mentioned.
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I'm looking for prepared a biodegradable composite, which will be made by natural fiber like sponge-gourd or jute fiber.
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For Cylindricity Measurement Apart from the Co-ordinate Measuring Machine, Which one is the best and easiest method for calculating the Cylindricity of the drilled Specimen. (Natural Fiber Reinforced Polymer Composites.)
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Please refer to this article, you will get some idea.
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Surface sizing agents are mostly amphiphilic molecules, having both hydrophilic (water-loving) and hydrophobic (water-repelling) ends. The sizing agent adheres to substrate fibers and forms a film, with the hydrophilic tail facing the fiber and the hydrophobic tail facing outwards, resulting in a smooth finish that tends to be water-repellent.
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Please refer to this article, you will get some idea.
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Dear researchers, I would like to use 3D printers to make samples in bio composites (PLA + Natural fibers). Do you have any idea.
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Good work. Thanks a lot for sharing this article.
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In a stress-strain curve of an FRP composite, mostly it is represented strain in terms of (%) rather than in (mm). Why it is represented in such a way?
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Strain is any kind of deformation, including elongation. Elongation is the word used if we're talking specifically about tensile strain which the sample deforms by stretching and becoming longer. Usually the percent elongation is calculated, which is just the length of the polymer sample after it is stretched (L), divided by the original length of the sample (L0), and then multiplied by 100.
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How much time remains between acceptance and production (author agreement) of the article in the journal of natural fibers ( Taylor & Francis).
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Thanks a lot for your replay
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powdered fibers or completed fibers(without being crushed and grinded)
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No thanks, though you didn't added more details, I extend a little bit my previous answer. If mechanical properties such as resistence in tension, fibers are more suitable, however if friction/abrasion is you goal, powdered reinforcing filler is to be used. Best of success in your work
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After alkaline treatment (various % concentrations) with Natural fiber, dry in the hot air oven at 70 degrees Celcius for 4hrs.
1). 'Na' is coated on the surface of the fiber. how a coating of 'Na ' Varies with the strength of Natural fiber
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Le traitement de la fibre végétale à la NaOH encore appelé mercerissage du nom de Jorn Mercer 1884 a pour rôle de renforcer la résistance de la fibre et de rendre la fibre brillante
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In order to give input during FE modelling of NFRPC, this value is required. How to determine? Kindly enlighten me.
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Thank you for your answers people
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We are trying to carry out surface modification (using alkali treatment) on selected natural fibres for use in cement matrix composites. However, some of our team members proposed using demineralized water for the treatment process in place of the commonly used distilled water. Several literatures have reported the use of distilled water in this process but as of today (29th June, 2021) and as much as I know, I have not seen/read any literature suggesting the use of demineralized water for this particular process.
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Always use distilled water for process purposes
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How to find density of natural fibers, which are also hydrophobic in nature and micro porous? Also when we use thermoplastic as matrix and natural fiber as reinforcement, the density of fiber may vary due to variation in inter-facial bonding and due to processing conditions. Then which value is to be considered as benchmark?
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There are five test methods:
- the diametral and linear density,
- Archimedes,
- helium pycnometry,
- the gradient column
- liquid pycnometry.
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I have prepared natural fiber reinforced polyolefin composite for which methane emission has to be estimated once it lands to landfill after completing the service life. Is there any article which talks about this or any methodology to estimate the green house gas emission specially methane.
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Thanks all for your valuable inputs.
Prof. Hatsuo, its a short fiber reinforced polyolefin composite. it would be great if you can advise any standard ASTM/ISO or research article dealing such kind of problem.
For landfill, is it the anaerobic degradation that we should look for?
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iam doing a simulation in ansys composite prepost for a natural fiber reinforced polymer composite.so in-order to obtain the numerical result i need to add the material properties for the woven fabric in ansys engineering data.so kindly please help me to find out the procedure for finding out the young's modulus , shear modulus, poisons ratio in x,y,z direction for the woven fabric material experimentally.
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You can use an online tool called TexGen4SC (https://cdmhub.org/resources/texgen4sc) to obtain all the properties numerically.
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Natural fibers are usually obtained by retting of stems of bast fiber yielding plants and then beating them manually or mechanically to separate the fibers. I would like to know if there is any method by which it can be done without the process of beating.
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You need some mechanical action to finish the separation even when bast fiber ribbons have been retted. You could pass the ribbons through fluted rollers; the finer the flutes the better the cleaning job but the lower the capacity. You could put the retted ribbons on a belt or slats with steel pins starting with coarse widely spaced pins and then passing to another pins with slighting finer more closely spaced pins and then to a belt with even finer pins and closer spacing. On top of these belts you have other pined belts that run slightly faster than the lower belts. The upper pins are set so they go between the lower pins. This gives a combing action and will pull apart retted bast bundles. You could also try a coarse garnet machine with very large drum and teeth; followed by one with finer teeth etc. In flax this is done with a "breaker card" followed by a "finisher card".
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In making of natural fiber based bio composite, researchers are looking for natural materials, in this context i want to know about the additives used to cure the matrix materials for biocomposites.
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I am also going to find the natural resins. However, as per my little experience I could suggest you to consider it like as other resins such as epoxy/MDI/PF with or without hardeners for composites manufacturing.
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what are wood plastic composites (WPCs)? Are the composites made with natural fibers and polymers comes under WPC category? why thermoplastic polymers are usually used for the synthesis of WPCs?
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Wood-plastic composites (WPCs) are produced by mixing ground wood particles and heated virgin or recycled thermoplastics including HDPE, LDPE, PVC, PP, ABS, PS, and PLA.
According to the WPCs' application, the mentioned thermoplastics can prepare desired properties.
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Dear network,
I am looking for the LCA or LCI or at least the energy balances of the non woven fabrics process for my master project, in specific for natural fibers, yet I have found difficulties in finding the proper information. If you have by any chance information or papers containing this kind of info, please let me know,
Thanks in advance
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ps: here you should find more info https://cfda.com
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I am working in polyester/ natural fiber composite—my research work is facing this trouble.
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if the quantity is enough you can use an extruding process to release the bubble from the polymer
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Hi everyone,
I am looking for a machine to grind the natural fibers for use in concrete (fiber reinforced concrete). I appreciate if you can suggest a good type or share your experiences in this case.
Best Regards,
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you can use also Las Anglos machine, and other blender machine.
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1. In a Low-velocity impact test, I have got Force vs Time response. There were two peaks in cross-ply and angle-ply orientation. In cross-ply, its peak to peak distance is lesser when compared to angle-ply. What is its significance?
2. Another was, steep rise in the cross-ply but the linear increment in angle -ply. What might be the reason?
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higher stiffness
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Looking for making a noble green composite (nano-biocomposite) by sponge-gourd (Luffa cylindrica) natural fiber, where PLA will be used as a matrix material.
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Have you considered grinding the luffa fiber material down to <200 nm, then mixing them into acetone and PLA solution and then spray drying the material? If done correctly you could end up with semi-porous PLA particles with uniformly dispersed nano-luffa fibers imbedded. You could then assemble the powder into the structure you wanted and add a little heat. Or you could melt it all into a wire and 3D print with it.
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How the diameter of the fiber plays a role in interfacial bonding? If the dia of Fiber is small, we assume the matrix will completely adhere to the fiber. If the dia is larger, the same matrix covers the fiber. Whatever the surface area might be. It depends on how good it binds the fibers. But how this dia play a role in that?
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In summary mechanical properties of thermoplastic fiber reinforced compounds are largely influenced by fiber orientation and fiber length retention ( shorter ones result in higher number of fiber ends, where premature failure of polymer matrix usually occurs) , that reflects low fiber breakages during processing and good fiber wetting ( to promote a continuous phase) . However these are opposing factors as good fiber orientation and wetting requires higher shear that causes fiber breakages. Thus to get a more appropriate balance one has to choose an appropriate screw configuration , and paly around extrusion residence time.
Other points to consider are :
. fiber properties
. fiber sizing ( that will react with adhesion promoters / coupling agents to result in a stronger interface between fiber and polymer matrix)
. type and amount of coupling agent
. kind of extruder used and screw configuration
. location of fiber let down in extruder
. extrusion residence time
. polymer viscosity ( will tend to affect wetting performance as well)
. the diameter of the fiber will affect the critical fiber length , defined as the minimum length required for the maximum fiber stress to achieve the ultimate fiber strength at its mid-length , estimated by :
*Lc = (Ultimate fiber tensile strength X fiber diameter )/ ( 2 x interfacial shear between the fiber and the matrix), under the assumption that both matrix and fibers show a linearly elastic responses.
* more details can be found :
. Kelly, A. and Tyson , W. R., J. Med. Phys. Solids, 13, 329 - 350 / 1965
. R.A. Malloy , plastic Part Design for Injection Molding , Hanser Publishers, New York, 1994, page 265.
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Papaya is a delicious fruit and vegetable contains  Vitamin A, Vitamin C and Vitamin K as well as potassium, magnesium, protein carotene and natural fiber. But not only in papaya, its seeds also have many qualities. Although its taste and smell a bit intense. Papaya seeds are full of phenolic and floboyed substances. It contains proteins, calcium, magnesium and phosphorus.
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Dear Dr Salma
papaya seed powder. Toxic reactions include; erratic movement, air gulping, loss of reflex, molting and discoloration. Maximum admissible toxicant concentrations ranged from 0.1 to 1.29 mg/L (confidence level: 22 - 78.8%).
Reference:
Toxicity of pawpaw (Carica papaya) seed powder to ...
www.academicjournals.org › app › webroot › article
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Hello,
I'm studying PhD at BarcelonaTech and I got the problem of the degradability of natural fibers in cementitious matrices.
So far, we got to protect the fiber usin resin, but I am looking for another solutions that can protect the fiber againts the alkaline attack.
I work with threads of natural fibers instead of only fibers.
Have some of you studied it?
Thank you in advance!
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Hi Alex,
The main purpose of the composite is to reinforce current damaged structures to increase the life of the building. As it is known that the alkaline environment speeds the degradation of the fiber we need to coat it with something that protects the fiber. At the same time, we need a good adhesion between the fiber-coating and mortar. Because if we do not have a good adhesion with the mortar, the composite won't perform as it is requested.
As we are not chemists, we decided to use epoxi resin in previous research, and at this point I have to keep it, but I think there are other options that might work better that epoxi resin (that is highly toxic and goes against our idea of a "more sustainable" technology).
I'm not sure about the exact pH of my mortar. I'll take a look. Thanks!
Thanks for the advice, while working with epoxi resin we go full protected, masks, glasses, gloves, lab coat ;)
See you,
Virginia
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How to determine cellulose, Hemi-cellulose, Lignin Content of natural fiber?...What type of chemical treatment should done to determine these contents....Please provide the details which you find very useful.
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There are chemical methods by which the chemical composition of the natural fibers can be determined. For example TAAPI procedure in which the individual components (alpha cellulose, hemicellulose and lignin) are separated and determined quantitatively. There are several research papers on the properties of natural fibers (such as Hildegardia populifolia uniaxial natural fabric, Tamarind Fruit fibers, Borassus fruit fibers, Ridge guard 3 dimensional fabrics etc) available in the literature which describe these procedures.
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Hi,
I am researching sustainable materials for product design. I would like to use liquid resins which are relatively easier to handle and can be used in multiple ways like natural fiber reinforcement and casting. At the same time, they should also be biodegradable. 
Thank you.
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Dear Karan,
There are two types of bioresin: degradable and compostable. Degradable bioresins can continually be broken down into smaller and smaller pieces—they are different from biogradable resins, because they cannot be reduced to simple biological matter. Compostable resins can be used as mulch after being mixed with specific bio products at a composting plant.
Please look at the paper
Cashew nut shell liquid-derived -Bio-based epoxy resin toughening with cashew nut shell liquid-derived resin resin(file:///C:/Users/3020/Cookies/Desktop/Downloads/GrMAT_2015.pdf), in this paper is nut shell- bio and liquid ester is a resin missed to form a bio resin.
Hope it help you out.
Ashish
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Whether Natural fibers be reinforced with Metal matrix to improve their properties? What kind of mechanism is involved in this?
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Thank you Prof. Thakur for your suggestions
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A Previous well-known technique is TG/DTg but the fibers decompose with the rubber on raising the temperature so it won't work what else characterization technique we can use for this particular.
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Dear Durmus,
I mean to say the chemical interactions between fiber and polymer chains.
which spectroscopic techniques can be used kindly give some references.
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I was doing a mixing of a natural fiber filler in a elastomer matrix before the mixing size 200 nm and after mixing i found the fiber particle size was reduced to 50 nm(With respect to SEM analysis) what may be the reason kindly suggest with reference.
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Mixing on a two roll mill? If so then there is a possibility of size reduction.
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Cellulose is normally crystalline in nature. I need to reduce the crystalline nature of cellulose extraced from natural fiber so that its thermal conductivity gets reduced.
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Dear All,
I have to perform natural fiber treatment.
I don't have the idea of how much quantity of fiber needs to be added to solution.
For e.g. if I have 1 litre of (5%NaOH + water) how much quantity of fiber can I add to it?
Please help me on this.
Thanks,
Gangadhar
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for research work
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Use any ceramics Nanoparticles.Ex. SiC, TiO2, ZnO. Definetely it will increase thermal properties of natural fiber reinforced PLA composites
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i am using short natural fibers for preparation a bio composite..i need to know what the range of fibers lengths
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I was asking if we could convert fibers into powder and what kind of techniques could be used.
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Use Universal Cutting mill machine..
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to enhance natural fiber one can use cross linking reaction mechanism with some chemicals, e.g potassium per manganate, formaldehyde citric acid etc. among these i need to know preferable ones.
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Dear Sir,
Please kindly go through this paper.
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The concentration of silane was fixed as the weight of silane relative to weight of fibres. Eg: In 5 wt% of silane solution, the 0.5 g of silane was dissolved in the ethanol/water solution for 10 g of fibres. So, is the amount of ethanol/water mixture important in silane treatment? Or the maximum amount of the mixture is 50 ml for 5 wt% of silane? Thank you very much
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Dear Mr. Thiago Felix,
Thank you for your feedback. I'm using APTES. I understand that ethanol/water is used to allow the hydrolysis of silane but I would like to know is there any negative effect if the amount of water is too high.
Thank you.
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what effect of natural fiber diameter on sound absorption in polyurethane composite foams?
Whatever the diameter of the fiber be lowered, the composite sound absorption will be better?
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if matrix concentration more low will be the NRC.
For fibre diameter, obvious fine will give more NRC.
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i want to use compression molding method to prepare a bio composite based on cornstarch as a matrix and some natural fibers (particulate) as a reinforcement
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Compression molding is essentially a typical squeezing flow operation. The constant normal load (compression pressure) can be calculated knowing the initial separation of the mold plates and the squeezing rate and the rheological properties of the material that is being molded. Expressions for circular disks and flat strips are available on pp. 246 -247 of the following book in the section that discusses compression molding (p. 244). This should give a fair idea of what best compression pressure value and time is needed for the specific material composition of interest.
A. V. Shenoy and D. R. Saini, Thermoplastic Melt Rheology and Processing, Marcel Dekker Inc., New York (1996).
Surface modifiers are used for ease of flow and protection against surface cracks/imperfections during processing, and for developing stronger interfacial bonds to improve the strength of the composite. Surface modifiers are system-specific and hence for a specific natural fiber cornstarch matrix biocomposite, the right one giving optimal properties needs to be found by some trial and error. Some of the typical surface modifiers that are used in the polymer industry for preparing filled polymer systems are discussed on pp.21-34 of the following book, and the surface modifier for the specific biocomposite can be chosen from one among them.
Aroon V. Shenoy, Rheology of Filled Polymer Systems, Kluwer Academic Publishers, Netherlands (1999).
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to my understanding it is a heat vaporization peak.But still i need more information regarding it.
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thank you so much Pierre caulet..
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I got an error in Ls Dyna after solving, says that *** improper format** and error in keyword.
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ash contents in chemical composition of natural fibers
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Ash content is the residue or the leftover after burning a known quantity of the material in question in muffle furnace at about 725 - 750 degrees for an hour and is attributed to inorganic mineral content which is not worth burning called as ash. It may be due to presence of metal oxides like silica or magnesia etc.
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XRD Peak intensity
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Increase of XRD peak intensity is a measure of increasing crystallinity. But you may share a bit more about your sample system.
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We are currently conducting a research project on Natural Fiber reinforced biopolymer composites (green biocomposites) for food packaging application. 
Previously, we did an experts' survey on weight of  importance for 13 selection criteria to find the most suitable natural fiber. From that survey and by applying AHP Rating Mode method, we found that the top 5 ranking of criteria based on their importance are:
Rank            Criterion
1                   Raw Cost (10.6%)
2                   Tensile Strength (9.7%)
3                   Young's Modulus (8.8%)
4                   Availability (8.8%)
5                   Moisture Content (8.7%)
Now, we are to find the most suitable biopolymer matrix which are among starch biopolymer alternatives i.e rice starch, potato starch, wheat potato, corn starch etc. Therefore, we have identified 19 selection criteria. We really appreciate your feedback in assigning a weight of importance out of 7  score on  1 -  7 scale (1 being the "Not at all important", and 7 being "Extremely important") for each criterion in evaluating starch alternatives. 
Please click the link below to participate in the Experts' Survey: https://goo.gl/forms/K5bVs1Hq7KIgk0V72 All data collected will be used ONLY for this research. 
We hope to gather feedback from all experts by 9th of January 2019. Your feedback is very valuable and all your cooperation are highly appreciated.
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criteria is the compaatbity of the reinfocement with the matrix.
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Length/diameter gives us the aspect ratio. Which value of the length should be consider physical length or microscopic?
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Alhayat Getu Temesgen See my answer above yours....
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Can we replace polythene bags by biodegradble materials specially made of speciality grade papers. If high strength kraft paper can be used for making low weights carry bags?
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In addition, I note the interesting discussion inspired me to the following considerations:
Is it necessary to improve the waste management technique?
I believe that it is necessary to apply appropriate waste management techniques due to the need to develop a new green economy, ie to implement the principles of sustainable development. It is necessary to minimize and limit the negative effects of climate change, generated by the progressive greenhouse effect of the Earth, which is rapidly accelerating global warming.
Improvement of waste management techniques should be implemented through the increase of automation, computerization and robotization in the field of planning and logistics of this process.
In view of the above, I would like to ask you: Is it necessary to improve the waste management technique?
Please, answer, comments. I invite you to the discussion
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Related paper on above if any
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The density, porosity, crystallinity, and reactivity of natural cellulose fibers are discussed in the below mentioned articles. Happy new year.
View full-text
Source
Article: On fine structure of cellulose fibers
Y Fahmy · F Mobarak
Full-text available · Article · Jan 1971 · Svensk Papperstidning
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how natural fibers reduce sound transmmision
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If you're interested in the way that different materials absorb sound, then the two properties of the material that contribute to this are its mass and elasticity. You can find tables of typical properties and absorption coefficients all over the web, such as:
and
Are you interested in a particular type/family of natural fiber?
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In recent years, the use of natural fibers in concrete is widely
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To specify the robustness of concrete. It is commonly used in the structural engineering. This is because for the following reasons: 1) high compressive strength, 2) low cost. 3) Plentiful raw material. As well, there are two main insufficiency: 1) low tensile strength. 2) Low strain at fracture
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I need to determine the stress-strain relationship of flax yarns. To calculate the nominal stress, I need to know the cross-sectional area (original area) of the flax yarn before the application of the tensile load. However, the cross-section of the flax yarn changes significantly when the yarn is pulled or straightened. Do you have any recommendation or reference for this?
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Dear
Md. Abdur Rahman
,
Thanks for sharing such a helpful link. In that link yarn linear density testing is recommended for measuring the cross-section area of the yarns. My yarns' length changes considerably from the situation the yarns are left loose to the situation that the yarns are stretched. Could you please advise how loose/tight the yarn should set (preferably in quantity) before measuring the length?
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I want to select natural fiber to develop biocomposite. I woud like to know which of the these fiber (Kenaf and pinnaple ) prove to have better strength over another
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There are numerous natural fiber available around the world. Strength of natural fiber varies significantly that depends upon the location and the chemical constituents that can be enhanced by treatment.
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Hi,
My name is Céeleste Robert and I am a master student at l'Université du Québec en Abitibi-Témiscamingue (UQAT). I am interested in your project as I am also working with PLA and natural fibers. I was wondering how your project is going. Have you encountered any difficulties while processing your composites? i am having some difficulties right now with the injection molding of my PLA. I started by practicing on the pure PLA, but they are giving me a lot of difficulties. The test specimen have defects in them and air bubbles. I tried tunnin many injection properties such as: the mold temp, the processing time and the time left in the mold before taking out the samples, the pressure, the injection time, and the injection temperature (nozzle and the different zones), but nothing seems to help.
Do you have any tips you could give me to make my injection adventure a little less chaotic? I am using a Haitian MA 600 II machine with a screw diameter of 24mm.
Thank you,
Céleste
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Dear Celeste, I observed this problem also in the past in my lab. Maybe interesting to think for additives that can optimize the processing. KR, Nabyl
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reinforced concrete
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As I know, some of the natural fibers used in concrete are cellulose fiber, sisal and coconut. But, must be chemically treated before use in concrete to ensure that it will not be decomposed.
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Hello All,
I am working on Natural Fiber PMC and I am not able to achieve stiffness, one of reason is the matrix being used has more flexibility.
Can you please suggest whether I have to go for filler addition or use any natural fiber which has high stiffness or go for hybrid?
If you know any natural fiber having better stiffness please suggest.
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Need articles on easy, economical and sustainable ways of preparation of Carbon from Natural fibers/ Products
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Looking too, so I am following.
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Can you please suggest labs or institutes where I can interact with the people to understand recent work carried out in Natural Fibers?.
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You should definitely check out the group of Sabu Thomas at Mahatma Gandhi University. They have been working in natural fibre composites since forever.