Download as pdf or txt
Download as pdf or txt
You are on page 1of 8

A study on various fire retardant additives

used for fire reinforced polymeric


composites
Cite as: AIP Conference Proceedings 2393, 020107 (2022); https://doi.org/10.1063/5.0074235
Published Online: 19 May 2022

Vishal Fegade, Krishnakumar Gupta, M. Ramachandran, et al.

ARTICLES YOU MAY BE INTERESTED IN

A review on basalt fibre reinforced polymeric composite materials


AIP Conference Proceedings 2393, 020172 (2022); https://doi.org/10.1063/5.0074178

A review on effect of cooling rate in fiber reinforced polymeric composites


AIP Conference Proceedings 2393, 020106 (2022); https://doi.org/10.1063/5.0074237

Preface: Recent Trends in Science and Engineering


AIP Conference Proceedings 2393, 010001 (2022); https://doi.org/10.1063/12.0006698

AIP Conference Proceedings 2393, 020107 (2022); https://doi.org/10.1063/5.0074235 2393, 020107

© 2022 Author(s).
A Study on Various Fire Retardant Additives Used For Fire
Reinforced Polymeric Composites
Vishal Fegade1, Krishnakumar Gupta1, M. Ramachandran2, a), S. Madhu3,
C. Sathiyaraj2, R. Kurinji malar2, M. Amudha2
1
SVKM’s NMIMS, MPSTME, Shirpur, Dhule, Maharashtra, India
2
REST Labs, Kaveripattinam, Krishnagiri, Tamil Nadu, India.
3
Saveetha School of Engineering, Chennai, India.
a)
Corresponding author: sweetestchandran@gmail.com
Abstract. The growing environmental awareness and natural resources scarcity various fully biodegradable polymer
systems development and utilization initiates poly lactic acid (PLA) and copolymers biodegradable polymer, extensive
attention as they biodegradability, numerous renewable sources, and excellent mechanical and thermal properties like
advantages other polyester resins like PLA inherent chemical composition and molecular structures due to very poor fire
resistance the aviation and electrical industry PLAs widespread use low thermal resistance, combustion and drip
hampered flame retardant modification essential Combustion-type flame retardants polymer by physical means
incorporated materials production convenient industry widely in used. Flame retardants certain chemical compounds
polymers paralytic reactions slow or inhibit or combustion oxidative reactions They mainly halogen, phosphorus and
metal hydroxides containing compounds Halogen flame retardant drawbacks metal components highlight ability
combustion during hydrogen formed toxicity and some governments or organizations halogen controlled flame retardants
use restrict proposed halogen-free flame-retardant additives indomethacin flame retardant (IFR) considerable attention
and polypropylene (PP) and polyethylene (PE) such as polymers used their low smoke, no toxicity, and halogen absence
benefits. and corrosive gas production In general an IFR system three basic components char-forming agent
carbonization catalyst, and a blowing agent combustion during IFR multi-cellular structure combustible layer a physical
that acts barrier gas and compressed between heat and mass transfer reducing reducing the burning melt in thermoplastic
flame-retardant conversion is a particular problem. Drops melting burning surface area increase fire intensity increase
faster fire spread viscosity Melting coal formation strong impact PLA, polyethylene terephthalate (PET), and poly
butylenes succinct (PBS) like Linear polymers branched or thermo set polymers compared low melt viscosity burning
test during serious melt dripping layered silicates thermal stability improve reduce filler concentration flammability
low investigations found.

INTRODUCTION
Fire fighting helps to slow down and prevent the spread of fire to reduce its intensity. It is a chemical reaction
that reduces the flame ability to delay the combustion of fuels. Chlorine and bromine are examples of allergenic
flame retardants. Phosphorus is used to produce liquid and solid organic or mineral flame retardants. Fire retardant
furniture, mattresses and thermal insulation materials Polyurethane foam to prepare flame retardant is used in.
retardant is defined as a substance that has been chemically treated for self-extinguishing. There are many textiles
that can be “treated”. If any object put in fire it will burn and turn to ashes. But asbestos is a non-combustible
material. The fire-fighter wear cloth made of asbestos and enters the burning house. In fact their clothing, shoes,
gloves, helmets, etc. are gradually excreted with fire-fighting chemicals called polyprominate biphenyl ethers or
PPDs because they are persistent in the environment, they have been found to be toxic to humans, and they
implicated in neuro developmental processes in neonates and in children. A household spray bottle can be used for
smaller ones, and unopened containers can last up to 10 years. The cost per drop is 65,000 to 22,000 per hour of
flight time. The heavy air tanker can carry about 3,000 gallons of retardant. The plan runs at a drop and
approximately 12,000 per flight time wool generally considered to be the most flame resistant natural fibers. Fire
extinguishers and chemicals designed to reduce the flame of commercial and consumer goods have been used for
decades in the country like United States of America and now all over the world. While fire fighters reduce the risk
of fire in many consumer goods, certain types of fire fighters can be harmful to the environment and human health.
"Seawater emits fire and fresh water, and although seawater is harder on pump equipment than fresh water, proper

Recent Trends in Science and Engineering


AIP Conf. Proc. 2393, 020107-1–020107-7; https://doi.org/10.1063/5.0074235
Published by AIP Publishing. 978-0-7354-4198-9/$30.00

020107-1
maintenance and system cleaning will limit their corrosive properties on our pumps."The fire department told Hank
in an email. In addition to gasoline and lighter liquids, alcohol abrasives, nail polish removers, hand sanitizers, and
ward removers can easily. The federal hazardous substance law, all flammable products must have a warning label.
If your home has a basement or play room. Ping pong balls fire waiting to catch. They are highly flammable and
they are made of celluloid. The celluloid is so concentrated that it does not take much to ignite the ping pong ball.
You may have a long list of flammable liquids in your home. In addition to gasoline and lighter liquids, alcohol
abrasives, nail polish removers, hand sanitizers, and ward removers can easily catch fire. But in the end it is the
consumer who has them responsibly to use. Cooking utensils and utensils can ignite a fire of some food and
products can help spread flames. Cooking oils such as citrus oil is highly flammable and can be dangerous if used
improperly. To protect yourself in your home avoid keeping smoke and flash dots in mind. Sugar and flour cooking
careful should be. The flour covers a large portion, Allows you to travel faster than flames. Since flour is a
carbohydrate, when it is mixed with air causing an explosion. In this we studied about flame retardancy, ammonium
polyphosphate, boric acid, magnesium hydroxide and zinc borate.

FLAME RETARDANCY
Polyethylene Terephthalate (PET) Terephthalic acid and ethylene Saturated with Glycol. Interested in recycling
PET mainly due to the widespread packaging from polymers, including bottles. [1] Since the mid-1970s, PET has
been used to make cold bottles the United States, first in Canada and Western Europe the increase is predicted after
its use in this area. The total global Consumption of PET is current is About 13 million tons, of which 9.5 million
tons were processed textile industry, which is used in the production of 2 million tons of audio and video tapes.
More than 1.5 million tons mainly used in bottles and jars in the production of various types of packaging. [2] The
high strength of the PET bottle has low weight and low penetration of gases (mainly CO2). Their aesthetic
appearance (good light transmission, smooth surface) is characterized by the most important feature of PET, which
determines its wide application in the packaging industry for their aesthetic appearance (good light transmission,
smooth surface) is characterized by the most important feature of PET, which determines its wide application in the
packaging industry for the food industry. [3] Halogenated retardants are widely used to catch free radicals.So,
eliminating the potential is spreading. An important issue for sustainable development in term of renewable
resources contain chemical. The use of renewable resources such as KF filler in the PP matrix is actively pursued
due to the improvement and biodegradability of a material. Plastic especially PP is widely used in industrial use such
as automotive, household and mineral water packaging, which contributes to a large percentage of household waste
and pollutes to environment. [4] This is because PP is indestructible. However, by adding natural fibbers to PP waste
it can be converted into other useful materials such as biodegradable, which have high economic value and protect
environmental awareness is currently increasing, non-biodegradable fibres such as carbon, glass, agamid and
biodegradable natural fibres such as hemp, flax, and sisal. There is a remarkable effort made by the technologist and
the scientist changes that. Like polymeric materials, these natural fibres burn very quickly, which materials is
essential for its safe service. [5] [6]. In this research, attempts have effect of treatment with flame retardant and
regression mechanisms of polymeric compounds, different approaches to the development of FR-compounds and
other hybrid properties, and with flame retardant agents. The preparation procedure of the mixture between the fibre
and the matrix, the treatment used to improve the adhesion of a plasma interface to the surface of the coconut fibres.
Coconut fibre-reinforced PLA compounds were prepared using the Cumming thread method. [7] The mechanical
properties of compounds such as tensile strength, Young's modulus and spacing Extension explored, and flame
retardant of samples the summary of the properties was measured. [8] These experiments, Effect of plasma therapy
and thermo behaviourfibres / PLA compounds. Layer double hydroxide (LTH) is synthetic ananic is a family of clay
containing host nano-layer material, consist of positive charge, interconnect Anan and water molecules. [9] LTHs
are their Distinctive chemistry and Due to layered properties. As flame retardant combinations used. Polypropylene,
EVA and of polyamide Improve fire resistance LTHs successfully Are used.

AMMONIUM POLYPHOSPHATE
Allergic Organic Compound is a fire retardant additive for their conventional antimony trioxide, used in
combination with compounds to improve their fire resistance performance (Synergistic effect of halogen metal).
When burned, they usually form halogen acid and metal highlights. [10] [11] The effectiveness fire extinguisher is
toxic gases and their known potential effect on formation of corrosive smoke against is always balanced. Passive fire

020107-2
extinguishers made of insulating systems (Formation of a carbonaceous charcoal in the substrate at the bottom of the
weld) steel structure. These materials are designed to reduce Heat transfer from fire. [12] [13] These settings
commonly called Mineral based or organic resin based products called intramuscular coatings. The steel integrity is
maintained for 1–3 hours and is designed to operate in extreme conditions for maintenance. This period is
considered sufficient to evacuate personnel and control the fire. Structural steel maintains its integrity 500C.Steel
structures above this temperature will collapse within minutes. Therefore, to ensure safety of steel structure, it is
necessary to maintain its temperature below 500 C during a fire accident. [14-15] The use of polygon such as
pentaerythritol, mannitol or sorbitol in intrinsic formulations for thermoplastics has been associated with
displacement and water solubility problems. Moreover, these additives are often incompatible with polymers and the
mechanical properties of the formulations are much later. [16] Those problems were solved by combining three
intrinsic flame retardant components into one molecule. Combustion-related accidents have always been a disaster
in human history. [17] Extensive fire protection measures nowadays new and modern prevention techniques have
arrived. All fire-related disasters of this day and age have been eliminated in major cities over the past centuries.
[18] Therefore, their fire behaviour prognosis and their structural improvement are, most importantly, at the design
stage with the addition of flame retardants, considering that consumption of polymeric materials made in the 21st
century has increased dramatically. [19] Melamine polyphosphate and zinc borate were analyzed in composite
methods with glass-fibre reinforced polyamide aluminium titilphosphine. Despite the high value of CO
concentration and smoke density, it is clear that PP has excellent ignition, especially in LOI and HRR. [20] By
adding the Mg (OH) 2 filler level to the internal fire extinguisher, the smoke density and CO concentration are
reduced and TTI is extended. If more Mg (OH) 2 is added to the mixture the main factor of tensile strength
decreases rapidly.

BORIC ACID
Although a catalyst proposed by some researchers, for such a chemical mechanism no direct test support was
provided. In which study, New for thermal analysis Test results, Cone calorimetric transformer spectrum (GC -
FDIR) analysis are provided, and the fire resistance method in wood is discussed. [21-25] Pass wood was treated
with boric acid, guaniluria Phosphate (GUP) and GUP-boric acid. The treated wood was then
analysedthermogrammetry (DG / DDG), differential thermal analysis (DTA) and cone GC-FDIR analysis. Thermo
grammar showed that bass wood treated with boric acid was three times more likely to lose weight than untreated or
GUP-treated wood. at 165C, which is GUP Standard. Boric acid DDA curve showed treatment pass wood had an
external heat at 420C; it refers to curing external polymerization reactions. Boric acid and GUP are significant in
wood. CONE results showed an integrated fire-fighting effect. Boric acid is produced from treated wood GC-FDIR
spectra indicates that the compounds are different from those produced from untreated wood. Boric acid reacts with
Dehydration and other oxygen removal reactions occur at relatively low temperatures (approximately 100–300C).
The isomerization of newly formed polymeric materials can be promoted by creating aromatic structures. [26] It
contributes in part to the effects of boric acid. Wood and wood-based products contain organic compounds, mainly
carbon and hydrogen, for this reason, they are flammable. Wood burning is advantageous when used as a fuel, but
not as a building material. [27] A tree cannot be made inappropriate, but it can be turned into fire. It is well known
that fire resistant boron compounds are effective as chemicals for cellulose products. [28] The boron-containing
compounds have been studied by many scientists for their fire-fighting properties and have been useful since the late
19th century. Boric acid and borax compounds have some effectiveness in preventing the spread of flames on wood
surfaces. In addition to the catalytic effect of conventional charcoal, they have a low melting point and can form
glass shapes when exposed to high temperatures in a fire. [29] Borax reduces flame spread, but does not smoke or
shine. Boric acid, on the other hand, suppresses smoking, but has little effect on flame spread. Therefore, these
compounds are commonly used together. The fire, mechanical and thermal properties of novel fire-retardant
compounds currently used in space are evaluated with conventional materials, i.e. epoxy-based materials for
structural parts and phenol-based materials for interior installation. [30] These newly developed materials (clean
resins and compounds) provide significant improvements in their properties by 40 to 70% without losing thermal
and mechanical behaviour. The most successful flame retardant combinations on the market today are flame
retardant combinations. [31] Can be physically introduced or reacted with a polymer chain. However, allergic
compounds can cause environmental and toxic effects. As a result of this environmental concern, flame retardant
boron compounds are one of the safest in current use and these or other industrial applications will not cause any or
any other harmful effects. The purpose of this study is to examine the effects of boric acid and borax and their

020107-3
combinations (PA / PX) on two fibre loads HDPE-based Properties of compounds. [32] Torque, flexibility And
attacking forces And torque and flexibility module Mechanical properties including; Oxygen index (LOI) And
controlling the burning rate Fire efficiency; With concentrated spruce wood flour Filled high density polyethylene
Thermal properties of compounds (DGA) and morphological properties (SEM and SEM-EDX) Were explored. [33]
this study, boron Leakage of compounds and hybrid specimens Its impact on LOI levels Easily due to leakage of
boron compounds Were examined. this study, leakage of boron compounds and its impact on the LOI levels of
mixed models were easily inspected due to leakage of boron compounds.

MAGNESIUM HYDROXIDE
The flame in the cable insulation material explored the use of magnesium hydroxide, which is cross-linked by
low-density polyethylene by saliva adhesive method. Different insulation contains magnesium hydroxide filled with
low density polyethylene. [34-37] According to the These body and Mechanical properties tensile strength,
interstitial Stretching, impact, bending, oxygen Code, smoke density, flammability, aging test, hot set test, standard
test method and ozone resistance. The determine test results Were analyzed the appropriate ratio of magnesium
hydroxide per cable insulation substance. Magnesium hydroxide ratio was found to provide Good material
properties that the insulation meets quality. Most regression However, these are additives in polymers that are
halogen based products. Systems are known for their corrosive, fuzzy and toxic fumes during combustion. [38]
Therefore, the current trend is aimed at limiting the use of halogen-based FR systems and research and development
is shifting towards halogen-free FR formulas. A solution is the addition of metal hydroxides such as magnesium
hydroxide to the polymer matrix. Previous studies have demonstrated that in many types of polymers (EVA, PVC,
nylon), especially in halogen-free systems, the use of a mixture of zinc borates with other same regressions has
major advantages. [39] Their action may be referred to as Smoke suppressant, after glow suppressant, corrosion
suppressant, tracking anti-inflammatory agent and, in some cases, synergistic agent. Reduction and replacement of
halogen flame reducers based on Toxicology and environmental aspects is in progress. [40] Red phosphorus is one
of the most environmentally because the incorporation and use of master patches has been successfully Established
to eliminate problems in dealing with security and stability. [41-45] Therefore, the biggest drawback to its
widespread use is Pr. Alternative flame retardant reddish-brown colour of polymeric material with. The following
are the most important factors in determining their effectiveness as fire extinguishers: (i) Endodermic decay,
approximately 180C to 350C for aluminium hydroxide and Magnesium hydroxide, the substrate of the soles of the
feet Heat dissipation. (ii) Inert gas during thermal breakdown (Water vapour) Release Fuel in the gas phase Dilutes
the supply. (iii) Heat to reduce substrate Fire-retardant additives available and harmful decay More on both products
Heat capacities for reduction. [46] Decomposition products from heat source Advanced of the substrate of the feet
Provide backup by promoting the formation of charcoal. It works by releasing endothermic decomposition and
compatible water at temperatures above 300C, forming an oxide residue that regulates heat feedback to the substrate
(about 60% by weight), which prevents the polymer from dripping during combustion and the amount of
combustible material. [47] Significantly reduces the effect of this addition on the thermal decomposition of the host
polymer, although the thermal decomposition of the pure polymers has received attention.

ZINC BORATE
The first recovered recycled plastics use to create product. Close loop recycle is the same recycled plastic is new
products that completely recycle plastic with its virgin oil. Ensures the product dilute continuously recycle and
recover material is added in same proportions. [48-50] Packaging products are a common practice for many PETs.
The first recovered Plastic is used for another product that is recycled called open-loop recycling. This doesn’t mean
new application has low value. Example textile fibre made from bottle-PET or printer components made from water-
bottle polycarbonate. The author identifies some challenge for the reuse of compounds: 1. the compounds are made
of Different matrix and Composition of reinforcement materials: Polymers, fiber reinforcements (Glass and carbon
fiber), and fillers (E.g. particles, fire retardants), Dyes etc.). 2. Compounds Honeycomb in general, Foam cores,
metal and ceramic tiles, Polymeric barrier films and in combination with other materials such as top coatings are
made. Due to cross links resins cannot be changed again. 4. [51] During the recycling process Pollution is a primary
May be the problem. 5. Collecting scrap materials, Deployment and Deploying is challenging and costly activities.
6. Lack of continuous supply of recyclables composites occasionally restricts long-term investment.7. Recycling
compounds Waste management can be developed using conventional methods problem due to liquid wastes (E.g.

020107-4
acids, bases, solvents and surfactants), gas and particulate emissions and solids wastes.8. Sometimes, it is difficult to
find workers who are qualified for long-term sustainable employment in the region. [52-55] One of the major
advantages of using cement-less concrete as a host material for GFRP waste bonding is the insurance that no
chemical incompatibility occurs due to the alkali-silica reaction. Under this perspective, the purpose of the current
mission is to explore a possible waste management solution for GFRP waste (by scarf, products and end-life
products) as a substitute for aggregate, aggregate or filler, based on the above studies. For this purpose, different
contents of recycled GFRP waste powder and fibers unique size quality, Sand accumulators and fillers were
incorporated into polyester based mortars substitutes. The added value of the recycling solution was estimated by the
flexibility and compression loading capacity of the GFRP attached mortars in relation to the unaltered simple
polymer mortars. One of the most popular and cost-effective techniques for continuous production of Structural
components with fiber reinforced polymer (FRP) continuous cross-section is Baltrusion (Bank, 2006; Stewart and
Some rack, 2000). [56] In general, in the production FRP stabilization Profiles, plain glass (GF), Carbon (CF) or
Aramide (AF) Reinforcing fibers are highly adhesive for enrichment Are pulled through the bath (Usually a poly-
ester, vinyl ester or epoxy resin), And moisturized After the process, the reinforcement will create a heat The motor
is allowed to enter, There it reaches the shape of a dead pit and heals. Finally, out of death, already integrated Mixed
area (GFRP, CFRP or AFRP profile) Pulls by continuous traction, then one saw the cuts area is desired for that area
Cuts Long. [57-60] Recycled FRP can be classified into two main groups: (1) retrieving fibres from Polymeric
matrix, and (2) mechanical recycling. Fibre regeneration involves the recovery of fibres from FRP, which can
usually be freed and collected by using an Aggressive thermal or chemical process thermo set matrix. Fibre
recycling Processes for carbon recycling can be attractive options fibre two reasons for Reinforced polymer (CFRP)
materials; (1) carbon fibres high chemical Have consistency, generally Their high mechanical properties are not
significantly affected during reassembly, and (2) Reconstruction processes are expensive and have only economic
justification for extracting expensive fibres such as carbon fibres. Many companies recover and reuse high-value
carbon fibre from CFRP waste. High-density polyethylene coated multivalent carbon nano tubes (C-MWNT) and
multifold carbon nano tubes (MWNT) are dispersed in ethylene vinyl acetate (EVA) polymer with mechanical resin.
The effect of C-MWNDs on tensile properties, thermo-oxidation decomposition and fire behaviour has been studied
in comparison with virgin EVA and EVA / MWNT nano composites. [61-62] Due to better dispersion of coated
nano tubes, the coupling of 3 wt% c-MWNTs leads to an increase in Young's modulus, synchronization of the
combustion residues and a decrease in the peak heat-output rate. Two main types of smoke suppression methods
have been proposed in rigid PVC for metallic compounds: one is the Lewis acid method 15 and the other is the
reduction bond method. They are all supported by some test results. [63] All metal compounds promote early cross-
linking of PVC increase charcoal formation during decomposition. Zinc-containing compounds are synthesized in
paralysis and PVC. [64] It is formed by the thermal decomposition of PVC in the Lewis acid mechanism. Which act
as excellent catalyst for ionic dehydro chlorination of PVC due to its strong Louis acidity.

CONCLUSION
Tips that helps to protect your home from fires. Check your electrical wiring is up-to-date, make sure to clean Your
Chimney Invariably, from your kitchen Remove irregular and flammable grease, Discuss fire safety with your entire family.
Bought a fire extinguisher Keep the discharges clear. Smoke detectors, Sprayers and fire Install the alarm system Grew
experiments with Mg (OH) 2 are the best results. These results show that amortardancy is mainly due to hydrated
filler displays, which cause decomposition. A mechanism for the action zinc boron can now be proposed. ADH
decomposes strongly through endo thermal reactions in Al 2 O 3, resulting in increased time. Beyond this time, the
polymer forms cross-linked network and carbonaceous charcoal. It controls the decomposition of the polymer.

REFERENCES
1. Liu, Ting, Jian Jing, Yan Zhang, and Zhengping Fang. RSC advances 8(8), 4483-4493 (2018).
2. Jang, Jyongsik, and EungKi Lee. Polymer Testing 20(1), 7-13 (2000).
3. Suharty, Nene Sri, Hanafi Ismail, KuncoroDihardjo, Muhammad Nizam, and MaulidanFirdaus. In Advanced
Materials Research,Trans Tech Publications Ltd950, 18-23(2014).

020107-5
4. Garcia, M., J. Hidalgo, I. Garmendia, and J. García-Jaca. Composites Part A: Applied Science and
Manufacturing 40(11), 1772-1776 (2009).
5. Jang, Jun Young, Tae KyeongJeong, Hwa Jin Oh, Jae RyounYoun, and Young Seok Song. Composites Part B:
Engineering 43(5), 2434-2438 (2012).
6. Jin, Xiaodong, XiaoyuGu, Chen, Wufei Tang, Hongfei Li, Xiaodong Liu, Serge Bourbigot, Zongwen Zhang,
Jun Sun, and Sheng Zhang. Journal of Materials Science 52(20), 12235-12250 (2017).
7. Li, Shumao, Hua Yuan, Tao Yu, Weizhong Yuan, and JieRen. Polymers for Advanced Technologies 20(12),
1114-1120 (2009).
8. Shumao, Li, RenJie, Yuan Hua, Yu Tao, and Yuan Weizhong. Polymer International 59(2), 242-248 (2010).
9. Fukushima, Kikku, Marius Murariu, Giovanni Camino, and Philippe Dubois. Polymer Degradation and
Stability 95(6), 1063-1076 (2010).
10. Chiu, Shih-Hsuan, and Wun-Ku Wang. Polymer 39(10), 1951-1955 (1998).
11. Wang, Qingwen, Jian Li, and Jerrold E. Winandy. Wood science and technology 38(5), 375-389 (2004).
12. Pan, Mingzhu, Changtong Mei, Jun Du, and Guochen Li. Composites Part A: Applied Science and
Manufacturing 66,128-134(2014).
13. Kanak Kalita, U Ragavendran, M. Ramachandran, Akash hoi, Structural Engineering and Mechanics, 69(1)21-
31 (2019)
14. M. Ramachandran, U. Ragavendran, Vishal Fegade, Fuzzy Systems and Data Mining IV: Proceedings of
FSDM 2018, 30961-67 (2018).
15. Sain, M., S. H. Park, F. Suhara, and S. Law. Polymer degradation and stability 83(2), 363-367 (2004).
16. Ramazani, SA Ahmad, ArashRahimi, MassoudFrounchi, and Saeed Radman. Materials & Design 29(5), 1051-
1056 (2008).
17. Fontaine, Gaelle, Serge Bourbigot, and Sophie Duquesne. Polymer Degradation and Stability 93(1) 68-76
(2008).
18. Braun, Ulrike, Bernhard Schartel, Mario A. Fichera, and Christian Jäger. Polymer Degradation and
Stability 92(8), 1528-1545 (2007).
19. Wesolek, D., and WeronikaGieparda. Journal of Nanomaterials (2014).
20. Chiu, Shih‐Hsuan, and Wu‐Kou Wang. Journal of Applied Polymer Science 67(6), 989-995 (1998).
21. Bar, Mahadev, R. Alagirusamy, and Apurba Das. Fibres and polymers 16(4), 705-717 (2015).
22. Colakoglu, Gürsel, SemraColak, Ismail Aydin, Umit C. Yildiz, and SibelYildiz. Silva Fennica 37(4), 505-510
(2003).
23. Ulla, Sami, Faiz Ahmad, Azmi M. Sheriff, Mohammad A. Bust am, GirmaGonfa, and Qandeel F. Gillani.
Progress in Organic Coatings 109, 70-82 (2017).
24. Zhan, Wang, Le Chen, Fusheng Cui, ZhaozhanGu, and Juncheng Jiang. Progress in Organic Coatings 140
(2020).
25. Kanak Kalita, M. Ramachandran, PramodRaichurkar, S. Haldar, Advanced Composites Letters, 25(4), (2016).
26. Cavdar, AyferDonmez, FatihMengeloğlu, and KadirKarakus. Measurement 60, 6-12(2015).
27. AyushChaturvedi, M. Ramachandran, Sunil Patil, International Journal of Mechanical and Production
Engineering Research and Development, 173-180 (2018)
28. ShubhamPaliwal, M. Ramachandran, Vishal Fegade, International Journal of Mechanical and Production
Engineering Research and Development, 83-86 (2018)
29. Cai, Yibing, Qufu Wei, Fenglin Huang, and WeidongGao. Applied Energy 85(8), 765-775 (2008).
30. Zhang, Zhen Xiu, Jin Zhang, Bing-Xue Lu, Zhen Xiang Xin, Chang Ki Kang, and Jin Kuk Kim. Composites
Part B: Engineering 43(2), 150-158(2012).
31. Sahas Bansal, M. Ramachandran, PramodRaichurkar, Materials Today: Proceedings, 4(2), 3182–3187. (2017)
32. Sener, Ahmet Akin, and EnverDemirhan. Materials & Design 29(7), 1376-1379 (2008).
33. Zhao, Chun-Xia, Ya Liu, De-Yi Wang, De-Long Wang, and Yu-Zhong Wang. Polymer Degradation and
Stability 93(7), 1323-1331 (2008).
34. Baysal, Ergun, Mustafa Kemal Yalinkilic, Mustafa Altinok, Abdullah Sonmez, HüseyinPeker, and Mehmet
Colak. Construction and Building Materials 21(9), 1879-1885 (2007).
35. Li, Zhenzhong, and Baojun Qu. Polymer Degradation and Stability 81(3), 401-408 (2003).
36. Marosfoi, B. B., S. Garas, B. Bodzay, F. Zubonyai, and G. Marosi. Polymers for Advanced Technologies 19(6),
693-700(2008).
37. Shajit Yadav, M.Ramachandran, Materials Today: Proceedings, 4(2), 1788–1793(2017)
38. Hornsby, Peter R., and Colin L. Watson. Polymer Degradation and Stability 30(1), 73-87(1990).

020107-6
39. Hornsby, P. R., J. Wang, R. Rothon, G. Jackson, G. Wilkinson, and K. Cossick. Polymer Degradation and
Stability 51(3), 235-249 (1996).
40. Durin‐France, A., L. Ferry, J‐M. Lopez Cuesta, and A. Crespy. Polymer International 49(10), 1101-1105
(2000).
41. P. M. Bhagwat, M. Ramachandran, PramodRaichurkar, Materials Today: Proceedings, 4(8), 1788–1793(2017).
42. Ning, Yong, and ShaoyunGuo. Journal of Applied Polymer Science 77(14), 3119-3127 (2000).
43. Genovese, Antonietta, and Robert A. Shanks. Polymer Degradation and Stability 92(1), 2-13 (2007).
44. Bourbigot, Serge, Michel Le Bras, Robert Leeuwendal, Kelvin K. Shen, and David Schubert. Polymer
degradation and stability 64(3), 419-425 (1999).
45. Marosfoi, B. B., S. Garas, B. Bodzay, F. Zubonyai, and G. Marosi. Polymers for Advanced Technologies 19(6),
693-700(2008).
46. U Ragavendran, Ranjan K. Ghadai, AkashBhoi, M. Ramachandran, Kanak Kalita, Transactions- Canadian
Society for Mechanical Engineering, 2018.
47. Hornsby, Peter R., and Colin L. Watson. Polymer Degradation and Stability 30(1), 73-87 (1990).
48. Hornsby, P. R., J. Wang, R. Rothon, G. Jackson, G. Wilkinson, and K. Cossick. Polymer Degradation and
Stability 51(3), 235-249 (1996).
49. Durin‐France, A., L. Ferry, J‐M. Lopez Cuesta, and A. Crespy. Polymer International 49(10), 1101-1105
(2000).
50. TejasShenoy, M. Ramachandran, International Journal of Mechanical and Production Engineering Research and
Development, 150-155 (2018)
51. YugalBagrecha, Raj Tailor, M. Ramachandran, P. Raichurkar, International Journal of Mechanical and
Production Engineering Research and Development, 150-155 (2018)
52. Ning, Yong, and ShaoyunGuo. Journal of Applied Polymer Science 77(14), 3119-3127 (2000).
53. Genovese, Antonietta, and Robert A. Shanks. Polymer Degradation and Stability 92(1), 2-13 (2007).
54. Bourbigot, Serge, Michel Le Bras, Robert Leeuwendal, Kelvin K. Shen, and David Schubert. Polymer
degradation and stability 64(3), 419-425 (1999).
55. Nie, Shibin, Chao Peng, Shujie Yuan, and Mingxu Zhang. Journal of thermal analysis and calorimetry 113(2),
865-871 (2013).
56. Kim, Sangcheol. Journal of Polymer Science Part B: Polymer Physics 41(9), 936-944 (2003).
57. Duquesne, S., F. Samyn, S. Bourbigot, P. Amigouet, F. Jouffret, and K. Shen. Polymers for Advanced
Technologies 19(6), 620-627 (2008).
58. DhruvMehendiratta, M. Ramachandran, International Journal of Mechanical and Production Engineering
Research and Development, 93-102 (2018)
59. PramodRaichurkar, M. Ramachandran, V. Subramanium, International Journal of Mechanical and Production
Engineering Research and Development, 103-108 (2018)
60. Zhang, Sheng, and A. Richard Horrocks. Progress in Polymer Science 28(11), 1517-1538 (2003).
61. Suppakarn, Nitinat, and KasamaJarukumjorn. Composites Part B: Engineering 40(7), 613-618(2009).
62. Arao, Yoshihiko, Sakae Nakamura, Yuta Tomita, KyouheiTakakuwa, Toshikazu Umemura, and Tatsuya
Tanaka. Polymer degradation and stability 100, 79-85(2014).
63. Asmatulu, Eylem, Janet Twomey, and Michael Overcash. Journal of Composite Materials 48(5), 593-608
(2014).
64. M. Ramachandran, JishnuPatil, Sidakdeep Singh Luthra, Ahmed Walija, International Journal of Mechanical
and Production Engineering Research and Development, 144-149 (2018)

020107-7

You might also like