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Effect of compaction on multi-physical properties of
hemp-black liquor composites
Marie Viel, Florence Collet, Christophe Lanos
To cite this version:
Marie Viel, Florence Collet, Christophe Lanos. Effect of compaction on multi-physical properties of
hemp-black liquor composites. Journal of Materials Research and Technology, Elsevier, 2020, 9 (2),
pp.2487-2494. �10.1016/j.jmrt.2019.12.079�. �hal-02562384�
w w w . j m r t . c o m . b r
Availableonlineatwww.sciencedirect.com
Original
Article
Effect
of
compaction
on
multi-physical
properties
of
hemp-black
liquor
composites
Marie
Viel
a,b,∗,
Florence
Collet
a,
Christophe
Lanos
aaUniversitédeRennes,LaboratoireGénieCiviletGénieMécanique,BP90422,Rennes,France bUniversitédeNantes,InstitutdeRechercheenGénieCiviletMécanique,BP92208,Nantes,France
a
r
t
i
c
l
e
i
n
f
o
Articlehistory:
Received8September2019
Accepted24December2019
Availableonline27January2020
Keywords:
Sustainablebuildingmaterials
Hempshiv
Thermalproperties
Mechanicalproperties
Moisturebuffervalue
a
b
s
t
r
a
c
t
Thisstudyaimstodevelopfullyagro-basedinsulatingbuildingmaterials.Previousstudies
investigatedseveraltypesofaggregatesandbinderstodevelopcomposites.Thethermal
conductivityofsuchcompositeappearsmainlyimpactedbythedensity.Thispaperaimsto
investigatetheeffectofdensityonvariousmulti-physicalpropertiesofcomposites,using
thesameformulationandadjustingtheformingstep.Thus,specimensareproducedwith
thesamehempshivtoblackliquorratiobutdifferentcompactionstress.Theeffectof
com-pactiononbulkdensity,porosity,mechanicalresistance,thermalconductivityandMoisture
BufferValue(MBV)isanalyzed.Itisshownthatitispossibletoreachthermalconductivity
thatislowenoughtobeconsideredasbuildinginsulatingmaterial.Thankstothisstudy,the
requiredcompactionstresstoensuretargetedvaluesofdensity,thenthermalconductivity
andMBV,isidentified.
©2020TheAuthors.PublishedbyElsevierB.V.Thisisanopenaccessarticleunderthe
CCBY-NC-NDlicense(http://creativecommons.org/licenses/by-nc-nd/4.0/).
1.
Introduction
Theagriculturalwastevaluationisoneofthecurrent
chal-lengesinthefieldofgreenbuildingmaterial[1–3].Agricultural
wastecanbeusedtoproducebio-basedpanelswithlow
envi-ronmental impact(embodied energy and carbon footprint)
andhighhygrothermalefficiency[2,4–6].Aspartofthe
ISO-BIOproject[7],thedevelopedthermalinsulatingpanelsare
ecofriendlycompositesmadeofaggregatescomingfromlocal
agricultureandgreenbinders.Thegluingeffectisobtainedby
couplingthermalandmechanicaltreatment.
∗ Correspondingauthor.
E-mails:marie.viel@univ-nantes.fr(M.Viel),florence.collet@univ-rennes1.fr(F.Collet),christophe.lanos@univ-rennes1.fr(C.Lanos).
In a previous study, presented in [8], various
compos-iteswereinvestigatedwithBiofibat® hempshivorcorncob
residuesasaggregates,andcorncobextract,flaxfinesextract,
blackliquor,BioChoice® ligninorPLAasbinders.Aftermixing,
thecompositesareproducedbycompactingandthen
heat-ingleadingtothegluingoftheaggregates.Thisstudyshowed
thatthedevelopedcompositeshadlowthermalconductivity
(rangingfrom0.067to0.148W/(m.K))andexcellentmoisture
bufferingability(MBV>2g/(m2.%RH)).More,thethermal
con-ductivityincreasedlinearlywithdensity,whateverthekindof
aggregateandofbinder.
https://doi.org/10.1016/j.jmrt.2019.12.079
2238-7854/©2020 The Authors. Publishedby Elsevier B.V. This isan open access articleunder the CC BY-NC-ND license (http://
2488
j mater res technol.2020;9(2):2487–2494Thedensityofcompositesismostlyimpliedbythe
com-pactionstressappliedduringtheirproduction,amongother
factors.Theinfluenceofcompactiononphysicalproperties
(density,thermalconductivityandcompressivestressin
par-ticular)ofcompositeshasbeenhighlightedbyBalciunas[9]
inthecaseofhemp-sapropel composites(sedimentrichin
organicmatter)compactedat20,40and60%oftheirinitial
volume.
Thisstudyfocusesonthecompositesobtainedwithhemp
shivandblackliquor.
Hemp shiv are lightweight aggregates withhigh
poros-ityandinterestinghygrothermalproperties[10].Thismakes
themperfectlysuitedforthedevelopmentofbio-based
insu-latingmaterials.Theyarethemostcommonlyusedaggregates
intheliteraturefortheproductionofbuildingmaterials[2].
Blackliquorisarenewablebinderfromlocalindustry,is
betterfortheenvironment(lessCO2emissionand
preserva-tionoffossilresources)thanusingpetroleum-basedbinder
(urea-formaldehyderesin orphenolic resin). More, the use
ofblackliquorleadstoabetterhygrothermalpropertiesof
bio-basedcompositesthantheuseofpetroleum-basedbinder
(polyvinylacetate)ashighlightedinpreviousstudy[11].Black
liquorisreadilyavailablecomponentsincetentonnesofblack
liquorareproducedpertonneofpulpusingtheKraftpulping
process[12,13].Currently,blackliquorismainlyusedforthe
productionofenergy.However,efficientenergyproductionis
cumbersomeandexpensive[12,14,15].Itistherefore
impor-tanttoseektoenhancethisco-productinadifferentway.Due
toitschemicalcomposition(Kraftlignin,polysaccharides,
aro-maticsandaliphaticscomponents),blackliquorrepresentsan
interestingalternativeforthesynthesisofsustainable
chem-icals[16–18].
Forthisstudy,thecompositesareproducedwiththesame
hempshivtoblackliquorratiobutsevendifferentcompaction
stressesappliedduringformingstep(15.6,31.2,62.5,125,250,
500and1000kPa).
Thus, this study investigates the effect of compaction
conditions on density, porosity, mechanical, thermal and
hygricperformancesofcomposites.Itwillthenbepossible
todefine productioncompaction regardingtarget valuesof
multi-physicalproperties.
2.
Materials
and
method
2.1. Rawmaterials
Thecompositesare producedwithBiofibat® hemp shiv as
aggregatesandblackliquorasbinder.
TheBiofibat® hempshivwere producedin2016yearby
CAVAC(Sainte-Gemme-la-Plaine,France).Itsparticlesize
dis-tributionwasdeterminedbyimageanalysisasdescribedby
Amzianeetal[19].Thelengthofhempshivrangesfroml10
=5.5mmtol90=19.4mm,withanmediumvaluel50of11.5
mm(Fig.1).Thewidthrangesfromrangesfromw10=1.7mm
tow90=4.8mm,withanmediumvaluew50of2.9mm.The
elongationratio(length/width)rangesfrom2.2to6.5.
Bulkhempshivhaveinterestingthermalproperties(with
athermalconductivitybetween48and59mW/(m.K)[9,20,10])
due to their low bulk density. They also show excellent
Fig.1–ParticlesizedistributionofBiofibat® hempshiv.
Table1–Chemicalcompositionofkraftblackliquor accordingtothesafetydatasheet.
Components Content(%inweight)
Alkalilignin 14.1 Carboxylicacid 1.1 Aceticacid 4 Formicacid 10 Hydroxideacid 2.8 Polysaccharides 5.4 Sulfate 3.4 Sulfur 8.3 Sodium 15.9 Othercomponents 35
abilitytoregulateambientrelativehumidity(MBVabout2.31 g/(m2.%RH)[10]).
Theblackliquorisalowcostby-productfrom thekraft
paperindustry[18].Itiscomposedofabout70%drymatter.
Itschemicalcompositionmainlyincludesligninandinorganic
componentswhichmainlycomefromthepaperindustry
pro-cess.Italsoincludesfewpolysaccharidesandsomearomatic
andaliphaticcomponents(Table1)[16,21].Fig.2isa
diagram-maticillustrationoftheblackliquorstructure.Durmazetal
andNayerietalalsoobservedthattheblackliquorprotectthe
ligno-cellulosicresourcesfromfungaldevelopment[17,22].
2.2. Composites
Foreachkindofcomposites,sixspecimens(10×10×10cm3)
areproduced.Threeofthemareusedforthermalandhygric
characterization,thethreeothersformechanical
characteri-zationandmeasurementofskeletondensity.Thesameblack
liquortohempshivdrymassratioof15%isused.Thisvalue
ischoseninordertoensureagoodcohesion[23].
Forpreparation,thehempshivaremixedwiththeblack
liquorinamixerwithaflatpaddleduring5minutes.Themix
issplitinto threepartstoproducethreespecimens.
Speci-mensare moldedandcompacted5timesusinganInstron
5988testingmachinefittedwithaupperplunger,toensurea
goodparticlesarrangement.Theyaremaintainedunder
com-pressionandheated(for2hoursat190◦C),cooledtoroom
Fig.2–Diagrammaticillustrationoftheblackliquor
structure[21].
Tostudytheeffectofcompactiononmulti-physical
prop-erties,sevencompactionlevelsareconsidered:15.6,31.2,62.5,
125,250,500and1000kPa.
2.3. Characterizationmethods
2.3.1. Densitiesandporosity
Thedensityistheratiooftheweighttothesizeofthe
speci-men(whichisapproximately10×10×10cm3).Theweightis
obtainedwithananalyticalbalance(SartoriusLP8200S,
Göt-tingen,Germany).Eachdimension(length,width,height)is
theaverageoffourvaluesmeasuredwithanelectroniccaliper
(readabilityof0.1mm).Itismeasuredonthesixspecimensof
eachkindofcomposite.
Theskeletondensity s istheratio oftheweighttothe
skeletonvolumeofthespecimen.Thismeasurementis
car-riedoutusingapycnometeraccordingtothestandardASTM
D854[24].Aknownmassmsampleofdryandcrumbled
com-posites(foravolumeofabout 200ml) isintroduced into a
pycnometerofabout600ml.Then,thepycnometerisfilled
withtoluene.Itisregularlyshakentoremoveairbubbles.After
ensuringthatnoairbubblesaretrappedbetweenthe
parti-cles,thepycnometeriscompletelyfilledwithtolueneandthe
volumeoftoluenedisplacedbythecrumblesampleVsampleis
determinedfollowingtheequation(1).Threemeasurements
areperformedforeachcomposite.
s= msample Vsample = msample Vpycno−Vtoluene = m2−m1 m4 water−m3−m2toluene (1) with:
• m1:massoftheemptypycnometerwithground-glass
stop-per;
• m2:massofthepycnometerwithground-glassstopperand
sample;
• m3:massofthepycnometercompletelyfilledwithtoluene
withground-glassstopperandsample;
• m4:massofthepycnometercompletelyfilledwithwater
withground-glassstopper;
• toluene:densityofthetolueneatthetemperatureofthe
mea-surement;
• water:densityofwateratthetemperatureofthe
measure-ment.
Thetotalporosityntofacompositeisthevolumeratioof
theporositytothetotalvolumeofthespecimen.Itisthen
relatedtoapperentandskeletondensityofcomposite
follow-ing(Equation(2)).
nt=
s−app
s (2)
with:
• s:densityoftheskeletonofthesample;
• app:densityofapparentdensityofthesample.
2.3.2. Mechanicalcharacterization
Foreachcomposite,acompressiontestisperformedonthree
specimensto determinethe averagecompressive strength.
The test is carried out on a testing machine (Zwick/Roell
2490
j mater res technol.2020;9(2):2487–2494ProLine,Metz,France)fittedwitha20kNloadcell(Zwick/Roell
XForce,Metz,France).Theloadisappliedonthespecimen,by
themonotonousdisplacementoftheuppersteelplatewith
cross-headspeedof0.05mms−1.
FollowingtherecommendationsoftheNFEN826standard
[25],the resultsofthe compressiontests arestudiedusing
stress-straincurvesasdescribedbyVieletal[8].
2.3.3. Thermalcharacterization
For each composite,the thermalconductivity ismeasured
three times on three pairs of specimensobtained by
cou-plingthreespecimens,withthehotwiretransientmethod[26]
usingcommercial “CTmeter”device (SMEE,Voiron,France).
Theheatingpowerandtimeare 142mWand 120seconds.
Previouslytothemeasurement,specimensarestabilizedat
(23◦C;drystate)andat(23◦C;50%RH).
Thedrystateisreachedafterthedryingofcompositesin
anovenat60◦Cuntiltheirmassstabilization(thevariation
mustbelowerthan0.1%betweentwoconsecutiveweighing
forthreeconsecutive weighingwitha 24-hourstime step).
Then,thecompositesareplacedindesiccatorat23◦C.The
measurementsareperformedoncetheweightstabilizationof
compositesisreached(samestabilizationcriterionas
previ-ously).Thestabilizationat(23◦C;50%RH)isperformedina
climatechamber.
2.3.4. Hygriccharacterization
Foreach composite,the moisturebuffervalueismeasured
onthreespecimens,accordingtotheNordtestprotocol[27].
Itrelates the amount ofmoistureuptakeor release tothe
exchangeareaasafunctionofrelativehumidity(Equation(3)).
MBV= m
A.(RHhigh−RHlow)
(3) with:
• MBV:moisturebuffervalue(g/(m2.%RH));
• m:moistureuptake/releaseduringtheperiod(g);
• A:opensurfacearea(m2);
• RHhigh/low:high/lowrelativehumiditylevel(%).
Specimens are sealed on all their surfaces except one.
Afterstabilizationat(23◦C;50%RH),therelativehumidityis
submittedtodailycyclicvariations:8/16hoursat75/33%RH
(absorption/desorption period), during 5 days in a climate
chamber(VötschVC4060,Balingen,Germany).
3.
Results
3.1. Densitiesandporosity
Table 2gives the physicalproperties of compositesversus
compactionstress.
Theapparentdensityofdevelopedcomposites,atdrystate,
rangesfrom128to247kg/m3.Itincreaseswiththecompaction
pressurefollowingthe equationgiveninFig.4withahigh
correlationcoefficient.So,itispossibletoidentifythe
com-pactionpressuretoapplyforatargetdensity.Thenon-linear
curvegivenbyFig.4isduetothemechanismsofcompaction
Table2–Effectofcompactiononapparentdensitiesat (23◦C;50%RH)and23◦C;drypoint),skeletondensity andporosityofcomposites.
p 23◦C−50%RH 23◦C−dry s ntot (kPa) (kg/m3) (kg/m3) (kg/m3) (%) 15.6 135.8±3.7 127.6±3.7 1345.2±46.4 90.5 31.2 144.4±3.8 135.3±3.6 1325.2±11.4 89.8 62.5 155.0±2.8 144.9±2.7 1294.2±5.4 88.8 125 171.6±1.2 160.3±1.2 1282.9±6.7 87.5 250 191.4±0.9 180.7±0.9 1211.0±7.2 85.1 500 229.4±3.3 213.7±3.1 1269.9±2.1 83.2 1000 265.9±1.3 247.0±1.6 1283.0±11.0 80.7
Fig.4–Apparentdensityofcompositesat(23◦C;drypoint) versusthepressureapplied(p)duringthecomposites process.
that take placeduring thecomposites production:(i) grain rearrangementand(ii)elasticandplasticdeformationsof par-ticles[28].TheCooper-Eatonmodelmakesitpossibletoclearly
distinguishthesetwophenomena[29].
Furthermore,the densityofcompositesincreases by7%
fromthedrypointtothewetpointat(23◦C;50%RH).
Thedevelopedcompositeshaveverysimilarskeleton
den-sitiesrangingfrom1211to1345kg/m3.Theaverageofthese
valuesis1300kg/m3withavariationof±3.33%.The
formula-tionsofthesevencompositesdevelopedinthispaperarethe
same,soitisconsistenttohavethesameskeletondensity.
Moreover,thehemp-starchcompositesdevelopedby
Bour-dotetal,haveaskeletondensityclosetothisvalue.Indeed,
theyhaveaskeletondensityof1249kg/m3withavariationof
±1.02%[30].
Sincetheskeletondensityisthesameforallcomposites,
thetotalporosityofthecompositesevolveslinearlywiththeir
apparentdensity,followingtherelationshipbetweenthese3
valuesgivenEquation(2),andashighlightedinFig.5.Atthe
drypointanditrangesfrom80.7%to90.5%.
3.2. Mechanicalresistance
Thedevelopedcompositesmadewithhempshivshow
com-pactingbehavior(continuousstressincreasedversusstrain
-Fig.6).Thus,themechanicalperformanceisgivenbythe
com-pressivestrengthobtainedforthelongitudinaldeformation
Fig.5–Porosityofthedevelopedcompositesversustheir
apparentdensityat(23◦C;drypoint).
Fig.6–Stress-straincurveofthecompositescompressedat
31.2kPaduringtheproductionprocess.
Table3–Stressat10%deformationforeachcomposites.
p(kPa) 23◦C−50%RH(kg/m3) 10%(kPa) h=3m(%) 15.6 134.7±3.0 54.6±10.8 0.50 31.2 144.9±1.2 87.7±0.1 0.28 62.5 150.6±0.4 105.7±6.2 0.24 125 169.1±1.4 194.8±12.9 0.19 250 203.2±1.1 230.1±6.5 0.22 500 221.8±3.8 613.3±7.8 0.09 1000 270.8±16.7 802.7±131.2 0.09
Table3and Fig.7showthemechanicalproperties
mea-suredoncomposites.
Foragivencompactionpressure(between15.6and500kPa)
duringthe productionofcomposites, theexperimental
val-uesareveryclosetoeachotherbetweenthethreespecimens.
Incontrast,thecompositescompressedat1000kPaduring
theproductionprocesshaveexperimentalvalueswithalarger
measurementdeviation(coefficientofvariationofabout16%)
duetoasignificantvariationinapparentdensitiesbetween
thethreespecimens.Thecompressivestrengthrangesfrom
55to803kPa.Thecompositecompressedat1000kPaduring
theproductionprocesshasthehighestcompressivestrength
and thecomposite compressedat15.6 kPahasthe lowest.
Fig.7underlinesthatcompressivestrength evolveslinearly
withbulkdensity.
Fig.7–Stressat10%deformationofthedeveloped
compositesversustheirapparentdensity.
Table4–Effectofcompactionandhumidity(dryand 50%RH)onthermalconductivityofhemp-blackliquor compositesat23◦C. p dry dry 50%RH 50%RH kPa (kg/m3) (mW/(m.K)) (kg/m3) (mW/(m.K)) 15.6 127.6 62.8 134.6 71.0 ±3.7 ±1.1 ±3.4 ±1.1 31.2 135.3 65.7 143.3 73.1 ±3.6 ±1.9 ±3.9 ±1.8 62.5 144.9 65.6 153.7 72.7 ±2.7 ±1.3 ±2.7 ±1.0 125 160.3 68.9 170.1 77.8 ±1.2 ±0.9 ±1.1 ±1.0 250 180.7 71.1 190.4 78.2 ±3.1 ±1.5 ±1.0 ±3.0 500 213.7 79.8 225.4 91 ±0.9 ±2.8 ±3.4 ±1.9 1000 247.0 93.2 258.8 101.5 ±1.6 ±1.9 ±1.6 ±1.8
For3metershighwall,thestressinducedbythe compos-itesdensityleadstoh=3mdeformationslowerthan0.50%.The mechanicalpropertiesmeettherequirementstobeusedas buildinginsulatingpanelswithoutcompactionrisk.
Balciunas et al[9] also noticedon hemp-saprobel
com-posites that the compressive strength (from broken before
measurementto2080kPa)increaseswiththeapparentdensity
ofcomposites(from157to401kg/m3).
3.3. Thermalconductivity
Thethermalconductivityofhemp-blackliquorcomposites
rangesfrom62.8to93.2mW/(m.K)atdrypointandfrom71.0to
101.5mW/(m.K)atwetpoint(Table4).Thecompositewiththe
lowestcompactionpressure(15.6kPa)meetstherequirements
tobeclassifiedasinsulatingbuildingmaterialsregardingthe
NFP75-101standard(<65mW/(m.K))[31].
Fig.8underlinesthatthethermalconductivityincreases
linearlywithdensitywithahighcorrelationcoefficient.More,
Fig.8alsohighlightsthattheslopeistwicetheslopeobtained
foragro-resources[10].Thismaybeattributedtotheaddition
ofbinderandthecompactionwhichreducesinter-particular
2492
j mater res technol.2020;9(2):2487–2494Fig.8–Thermalconductivityofhemp-blackliquor
compositesversustheirapparentdensity:(a)Comparison
betweenthecomposites(yellowcurve)andthe
agro-resourcesinbulk(greencurve[10])atdrypointand(b)
Comparisonofthermalconductivityvaluesbetweendry
point(yellowcurve)andwetpoint(orangecurve).
Table5–EffectofcompactiononMBVofcomposites (averagevalueandstandarddeviation).
p MBVabs MBVdes MBVav (kPa) (g/(m2.%RH)) (g/(m2.%RH)) (g/(m2.%RH)) 15.6 2.50±0.03 2.77±0.02 2.63±0.02 31.2 2.60±0.09 2.86±0.09 2.73±0.09 62.5 2.82±0.11 3.06±0.11 2.94±0.11 125 2.63±0.07 2.87±0.06 2.75±0.06 500 2.31±0.01 2.49±0.01 2.40±0.01 1000 2.31±0.12 2.49±0.10 2.40±0.11
regression,it ispossibletoidentifythe requireddensity to reachatargetthermalconductivity.
Thethermalconductivityatwetpointisabout10%higher thanthethermalconductivityatdrypoint.Theslopeversus densityremainsthesame.
Balciunasetal[9]hadthesamefindingsonhemp-saprobel
compositesthatthethermalconductivityincreaseswiththe
apparentdensityofcomposite(=53to73mW/(m.K)for=
147to401kg/m3).
3.4. Moisturebuffervalue(MBV)
Following Table 5, the MBV ranges from 2.40 to 2.94
g/(m2.%RH).Allthecompositesareexcellenthygricregulators
accordingtotheNordtestclassification(MBV>2g/(m2.%RH))
[27].
Fig.9–MBVofhemp-blackliquorcompositesversus
density.
ThelowestMBVisobtainedforthetwocompositeswiththe
highestdensities(compactedat500and1000kPa).Thehighest
MBVisobtainedforthecompositecompactedat62.5kPa.Fig.9
givestheMBVversustheapparentdensityofcomposites.
Inafirsttime, theMBVincreasesupto2.94g/(m2.%RH)
foradensityof170kg/m3.Then,itdecreases downto2.40
g/(m2.%RH)fordensityof200kg/m3.Finally,theMBVremains
constant.Suchevolutionmaybeexplained:
• Inafirsttime,bytheincreaseinspecificsurfaceareawith
densitywhichleadstohighersorptionandthushigherMBV;
• Then, bythe decrease in vapor permeability induced by
lower inter-particular porosity which reduces the vapor
penetrationinthecomposite,andthustheMBV.
Thecombinationofthesetwoparametersleadsto
iden-tify anoptimumvalue ofdensity,and thus of compaction
pressure.Inordertovalidatethesehypothesis,
complemen-taryinvestigationsregardingvaporpermeabilityandspecific
surfaceareaarerequired.
BourdotetalfindthesameMBVwithhemp-starch
com-posites.Indeed,thesecompositeshaveanaverageMBVof2.63
g/(m2.%RH)foranaveragedensityof136kg/m3[30].However,
MaaloufetalfindaslightlylowerMBVwithalsohemp-starch
composites.ThesecompositeshaveanaverageMBVof2.46
g/(m2.%RH)foranaveragedensityof170kg/m3[32].
ColletandalfindalowerMBVrangingfrom1.94to2.15
g/(m2.%RH)forthehempconcreteswhichhaveadensity
rang-ingfrom430to460kg/m3[33].Thisdifferencecanbeexplained
bytheuseoflessbinderinthecaseofthecomposites
devel-opedinthispaper.
4.
Conclusion
Thedevelopedcompositesareproducedwithhempshivand
blackliquorwithseveralcompactionpressures.
Thecompositesdensityrangesfrom128to347kg/m3at
drystate.Thedensityiscorrelatedtothecompactionpressure
appliedduringtheproduction.Regardingthetotalporosityof
thecomposites,itisinverselyproportionaltotheirapparent
Thethermalconductivityincreaseslinearlywithdensity
between62.8and93.2mW/(m.K)atdrystate(23◦C;0%RH)and
between71.0to101.5mW/(m.K)atwetpoint(23◦C;50%RH).
Allthedevelopedcompositesareexcellenthygric
regula-torsastheirMBVranges from2.40to2.94g/(m2.%RH). The
MBVevolves with densityand shows anoptimalvalue for
densityaround170kg/m3.
Amongdevelopedcomposites,thecompositewiththe
low-estdensityshowshighthermalandhygricperformances.On
the one hand,its thermal conductivity meets the
require-mentstomakeitconsideredasinsulatingbuildingmaterial.
Ontheotherhand,itisanexcellenthygricregulator,withMBV
of2.77g/(m2.%RH)andhassufficientmechanicalproperties
foritsuse(selfbearingmaterials).
Acknowledgments
ThisprojecthasreceivedfundingfromtheEuropeanUnion’s
Horizon2020researchand innovationprogramundergrant
agreementNo.636835–Theauthorswouldliketothankthem.
CAVAC,industrialpartneroftheISOBIOproject,is
grate-fullyacknowledgedbytheauthorsforprovidingrawmaterials.
ThanksareduetoTonyHautecoeurforhisparticipationin
thecompletionofthiswork.ThanksareduetoYannLecieux
(Mechanicaltests).ThanksarealsoduetoCélineLeutellierfor
havingreviewedtheEnglishlanguage.
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