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TABLE of CONTENTS - brenntag.com · 3 Company Description InChem Corp is a global specialty resin...

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TABLE of CONTENTS

InChem Corp ...................................................................................... 3Introduction ......................................................................................... 5

Product Listings

Phenoxy Resin Products .............................................................. 6 - 13

Application Guidelines

Performance/Technology/Chemistry .................................................. 14Coatings & Inks Selection Guide .................................................. 5 - 16Adhesives Selection Guide ........................................................ 17 - 18Composites Selection Guide ..................................................... 19 - 20Plastics Selection Guide ............................................................ 21 - 22

Charts & Tables

Phenoxy Solution Viscosities ..................................................... 23 - 25Phenoxy Solvent Table ...................................................................... 26Phenoxy Physical Properties ...................................... inside back cover

PKFE, PKHC, PKHH, PKHJ, PKHM, PKHS and PKHW are registered trademarks of InChem Corp. We urgeyou to review prior to any use the Material Safety Data Sheets for any InChem Corp products mentionedherein. These documents are available from your InChem Corp Sales Representative or distributor. Thisinformation is not to be taken as a warranty or representation for which we assume legal responsibility nor aspermission or recommendation to practice any patented invention without a license. It is offered solely foryour consideration, investigation and verification. 2002 InChem Corp.

3

Company Description

InChem Corp is a global specialty resin andsurfactant manufacturer. Many of our resins havebeen used to enhance performance in coatings,inks, adhesives, and composites for over 35 yearsand they continue to offer unique chemistries toever-changing performance standards.

Our headquarters and ISO 9002 certified facility inRock Hill, South Carolina service customers world-wide along with additional production facilities inEurope. InChem surfactant facilities are located inPortugal, France, and South Africa.

Markets Served

The InChem resin product line services can andcontainer coatings, wire coatings, fiber sizings, inks,adhesives, composites and plastics manufactur-ing. We have direct sales and distribution through-out North America, Asia, Europe and the MiddleEast. At InChem new product development is thenorm, not the exception. We foster an environ-ment where creativity is encouraged.

Technologies

We have modified the Phenoxy molecule to offerits superior adhesion, flexibility and chemical re-sistance properties to water and solvent-borne,powder, UV, EB and cationic cure systems. Wealso offer very low viscosity epoxy acrylates andepoxy methacrylates.

Technical Services

We have extensive technical capabilities in ourR&D and QC/QA laboratories. Our technical staffare experts in their respective fields and are readilyavailable to help solve the most challenging appli-cation problems.

Major Products

InChem produces the following chemicals alongwith their derivatives:

Phenoxy (Polyhydroxyether)Epoxy Acrylates and MethacrylatesPolyesters

4

North America

Canada Colors & Chemicals Limited80 Scarsdale Road, Don MillsOntario M3B 2R7 Ph: 416-449-2600

Eastech Chemical Inc.5700 Tacony St.Philadelphia, PA 19135 Ph: 215-537-1000

E.T. Horn Company16141 Heron AvenueLa Mirada, CA 90638 Ph: 714-523-8050

Lintech International7705 N.E. Industrial Blvd.Macon, GA 31297 Ph: 800-652-9297

Maroon Inc.1390 Jaycox RoadAvon, OH 44011 Ph: 440-937-1000

Matteson-Ridolfi14450 King RoadRiverview, MI 48192 Ph: 734-479-4500

Mozel Incorporated1900 West Gate DriveColumbia, IL 62336 Ph: 618-281-2723

P.T. Hutchins (for Mexico)6055 E. Washington Blvd.Los Angeles, CA 90040 Ph: 323-887-8508

Europe

Brenntag Eurochem GmbHHumboldtring 15, D45472Mulheim an der RuhrGermany Ph: (49) 208-782-8144

Group Arnaud68 Av. du General Michel Bizot75012, Paris, France Ph: (33) 1-4473-1000

Hubron Specialty Products Ltd.Albion Street, Failsworth ManchesterM350FP, England Ph: (44) 161-681-2691

Europe cont.

Organa ChemplastVia Leonardo Da Vinci 4320090 Trezzano, sul NaviglicMilan, Italy Ph: (39) 02-4861-5352

Quimidroga S.A.Tuset, 26 08006Barcelona, Spain Ph: (34) 93-236-3636

Asia

Barrington ChemicalsRoom 13, 10/F New Commerce Center19 Sum StreetShatin, Hong Kong Ph: (852) 2547-5190

Kem Kote Ltd.100/78 Moo 4, Phuttamonthon 2North Bangkhae, Bangkhae, Bangkok10160 Thailand Ph: (66) 2-454-5100

Kingyorker EnterprisesNo. 58, 10th floor, Fu-Hsin North RoadTaipei, Taiwan Ph: (886) 2-2777-2369

Sine CorporationChoong Ang Royal Officetel, Room 14081355-8 Seocho-Dong, Seocho-KuSeoul, Korea Ph: (82) 2-3474-1188

Tomoe EngineeringDaini Maruzen Building, 9-2 Nihonbashi 3-Chome, Chuo-Ku, Tokyo103 Japan Ph: (81) 3-3274-0411

T.R. Chemicals Pty. Ltd.195 Briens Road, Northmead, N.S.W. 2152Australia Ph: (612) 9630-7655

InChem Corp Home Office800 Cel-River RoadRock Hill, South Carolina 29730

Customer Service: 803-329-8061Technical Service: 803-329-8050

also find us on the Web at: www.phenoxy.com

WORLD WIDE DISTRIBUTION

Rick
www.phenoxy.com

5

Introduction

InChemRez Phenoxy resins are tough and duc-tile thermoplastic materials having high cohesivestrength and good impact resistance. The back-bone ether linkages and pendant hydroxyl groupspromote wetting and bonding to polar substratesand fillers. Structurally, Phenoxy resin is apolyhydroxyether having terminal alpha-glycolgroups. Weight-average molecular weight rangefrom approximately 25,000 to above 60,000. Thehighest polymeric species exceed 250,000daltons.

Polydispersity is very narrow, typically less than4.0. An average molecule contains forty or moreregularly spaced hydroxyl groups suitable forcrosslinking for thermoset applications. These pen-dant hydroxyls are excellent sites for crosslink-ingin thermoset applications at elevated temperaturesand even at ambient conditions.

Phenoxy resins are compatible with many poly-mers and they are efficient flexibilizers forcrosslinked phenolic and epoxy formulations in ad-hesives, coatings, and composites. Phenoxy res-ins have shown utility in compatibilizing blends ofdiverse plastic materials. Phenoxy resin has asolubility parameter of 10.68 enabling excellent com-patibility with polar materials and sufaces like poly-urethanes, polyesters, and nylons. Generally, theresin is incompatible with acrylics, olefins, and vi-nyls. Phenoxy has excellent vapor barrier properies(water vapor, oxygen, carbon dioxide) and is com-pliant with 21CFR175.300 for direct and indirect food/beverage container coatings, as well as other para-graphs pertinent to adhesives used in multilayerpackaging and plastic components for containers.

InChemRez resins of Phenoxy type resins comb-ined with epoxies, polyethers, and polyesters pro-vide user friendly hybrids for formulation latitudeand novel properties.

Modification of the Phenoxy resin backbone bygrafting onto the aliphatic carbon segments gener-ates the family of anionically stabilized waterbornedispersions. These grades of Phenoxy (PKHW-series) allow formulators significant latitude in de-signing VOC compliant coatings and adhesives.Several are also FDA-compliant for use in packag-ing and container coatings (direct and indirect foodcontact).

Modification by esterification of the backbone hy-droxyls generates a new family of high molecularweight resins having pendant primary hydroxyls,vastly improved compatibility with ester-type sol-vents, and improved elasticity. Products of thistype are in the PKCP-series. These resins are notFDA-compliant however.

Phenoxy resins are soluble in a variety of materi-als including ketones, glycol ethers and glycol etheresters. Phenoxy resins prefer polar aprotic sol-vents, however many aliphatic and aromatic mate-rials will behave as diluents in conjunction withstrong solvents as above. Detailed solids/viscos-ity charts are illustrated in this guide for numeroussolvents and solvent combinations with differentgrades of Phenoxy.

Standard solutions of Phenoxy resin in methylethyl ketone and in PM acetate are commerciallyavailable from InChem Corp. InChem Corp. willconsider alternate solvents for customer specificneeds based on fit, volume, etc.

OHO C C C OH

OH HO C C C O

n

6

INCHEMREZ PHENOXY RESINSSTANDARD SOLID GRADES

ytisocsiV 1 Pc,52ta oC

sdiloS 2,%.tw

roloC 1,AHPA

ezaH 1,% mroFlacisyhP ,).va(nM

snotlad,).va(wM

snotlad

noitacificeps noitacificeps .ceps .ceps noitacificeps lacipyt lacipyt

BHKP 082-081 .nim99 .xam002 .xam51 stellep 005,9 000,23

+BHKP 904-182 .nim99 .xam002 .xam51 stellep 005,01 000,73

CHKP 425-014 .nim99 .xam002 .xam51 stellep 000,11 000,34

HHKP 517-525 .nim99 .xam002 .xam51 stellep 000,31 000,25

JHKP 577-006 .nim99 .xam002 .xam51 stellep 000,61 000,75

EFKP 598-006 .nim99 3 .xam002 .xam51 stellep 000,61 000,06

002-PHKP 517-574 .nim99 .xam002 .xam51 redwop 000,31 000,25

08-PHKP 517-574 .nim99 .xam002 .xam51 redwop 000,31 000,25

001-BHKP 904-081 .nim99 .xam002 .xam51 redwop 000,01 000,53

003-BHKP 904-081 .nim99 .xam002 .xam51 redwop 000,01 000,53

Pc,ytisocsiV52ta oC

,sdiloS%.tw

,roloCrendraG

,ezaH% mroFlacisyhP ).va(nM 4,

snotlad).va(wM 4,snotlad

noitacificeps noitacificeps .ceps .ceps noitacificeps lacipyt lacipyt

AMP03-SHKP 000,51-000,5 0.13-0.92 .xam1 .xam51 suocsivdiuqil 000,11 000,34

04-SHKP 000,7-005,4 0.14-0.93 .xam1 .xam51 suocsivdiuqil 000,31 000,25

1 20% solution in cyclohexanone 2 gravimetric, 3 hours at 135oC3 gravimetric, 3 hours at 80oC, then 1 hour at 220oC

STANDARD SOLUTION GRADES

4 on polymeric portion (GPC, versus polystyrene)

7

,gT o ,C)CSD(

xednItleM002ta oC

ytisocsiVtleM 5,002taesioP oC

cificepSytivarg 6 stnemmoC

lacipyt lacipyt lacipyt lacipyt

48 .nim01/g06 211 81.1 elbaliavaedargthgiewralucelomtsewolehT

78 03< ----- 81.1 edargthgiewralucelomwol-muideM

98 51< ----- 81.1 edargthgiewralucelommuidemesopruplareneG

29 4 564 81.1 snoitacilppatsomrofedargdradnatS

59 4< ----- 81.1 edargthgiewralucelomhgih-muideM

89 4< ----- 81.1 noisurtxemlifrof;edargthgiewralucelomhgih-artlU

29 4 564 81.1 .vanorcim011;snorcim002<;edargHHKPdezinorciM

29 4 564 81.1 .vanorcim06;snorcim08<;edargHHKPdezinorciM

68 06-03 ----- 81.1 .vanorcim06;snorcim001<;edarg+B/BHKPdezinorciM

68 06-03 ----- 81.1 egnarnorcim003ot051;edarg+B/BHKPdezinorciM

,.tPgnilioBoC

,.tPhsalFo CCMP,F

tnevloS]#SAC[

cificepSytivarg stnemmoC

lacipyt lacipyt noitacificeps lacipyt

531 411 etatecaMP]6-56-081[ 30.1 yxonehPedargCHKPfonoituloS

08 12 KEM]3-39-87[ 569.0 edargHHKPfonoituloS

Phenoxy Resin Polymers shownbelow are TSCA listed

as CAS# 25068-38-6

Theoretical OH equivalent weight: 284

INCHEMREZ NOTES

5 at 1034 s-1 6 fused, at 25oC

Special solvent packages with Phenoxy resins available on request (drums and/or bulk)

INCHEMREZ NOTES

8

INCHEMREZ PHENOXY RESINS

ytisocsiV 1 Pc,52ta oC

sdiloS 2,%.tw Hp eziSelcitraP

snorcimlacisyhP

mroF,.oNdicA

)sdilos(

noitacificeps noitacificeps .ceps .lacipyt noitacificeps lacipyt

53-WHKP 000,4-005,1 0.23-0.03 8.7-8.6 5.1 noisrepsidladiolloc 75

43-WHKP 006,1-008 0.53-0.33 8.7-8.6 90.0 noisrepsidladiolloc 74

63-WHKP 005,6-005,3 3 0.43-0.23 8.7-8.6 11.0 noisrepsidladiolloc 05

ytisocsiV 4 Pc,52ta oC

sdiloS 5,%.tw

roloC 4,AHPA

ezaH 4,%

lacisyhPmroF

lyxordyHrebmun

noitacificeps noitacificeps .ceps .ceps noitacificeps lacipyt

03-MHKP 003-001 .nim99 .xam002 .xam51 stellep 751

103-MHKP 003-001 .nim99 .xam002 .xam51 stellep 261

58-MHKP -000,03 000,05 6 .nim99 .xam001 A/N diuqilsuocsiv 012

38-MHKP 000,55-000,53 6 .nim99 .xam001 A/N diuqilsuocsiv 771

Pc,ytisocsiV04ta oC

tnecrePyxonehP)sdilos(

,sdiloS%.tw EPW mroFlacisyhP ,roloC

rendraG

noitacificeps lacipyt lacipyt .ceps noitacificeps .ceps

BH-REL 000,05-000,02 01 001 412-202 diuqilsuocsiv .xam2

HH-REL .nim000,53 01 001 412-202 diuqilsuocsiv .xam2

BH-NEL 000,54-000,03 01 001 691-281 diuqilsuocsiv .xam2

VLBH-NEL 000,61-000,11 01 001 691-281 diuqilsuocsiv .xam2

WBH-REL 0007-0005 7 01 38 572-552 diuqilsuocsiv noisrepsid

PHENOXY/POLYESTER BLENDS

LIQUID EPOXY/PHENOXY BLENDS

1 Brookfield RVT, #4 at 50 rpm 2 gravimetric, 1 hours at 200oC3 Brookfield RVT, #4 at 20 rpm

4 20% solution in cyclohexanone 5 gravimetric, 3 hours at 135oC6 Brookfield RVT 7 (below) at 25oC

WATERBORNE DISPERSIONS

9

s'COV.lag/blni stnevlos-oC gnizilartueN

enima stnemmoC

lacipyt noitacificeps noitacificeps

0.2 rehtelytublocylgenelyhte AEMD 8 snoitalumroftesomrehtrofnoisrepsiddradnatS

0.2 PnP;HOuB-n 7 AEMD stnevlos-ocPAH-non;noisrepsideziselcitrapwol-artlU

0.2 PnP;HOuB-n AET 9 snoitalumrofgniructneibmarofgTwoL

s'COV.lag/blni

lyxordyH1(rebmun o)

).clac(

cificepSytivarg stnemmoC

lacipyt lacipyt lacipyt

0 9 91.1 loylopepyt-retseylophtiwyollaedarg-diloS

0 41 91.1 loylopepyt-retseylophtiwyollaedarg-diloS

0 081 01.1 loylopepyt-retseylophtiwerutximedarg-diuqiL

0 441 20.1 loylopepyt-rehteylophtiwerutximedarg-diuqiL

s'COV.lag/blni

ytilanoitcnuF)tnenopmocyxopE(

cificepSytivarg stnemmoC

lacipyt lacipyt lacipyt

0 2 81.1 BHKPyxonehPhtiwdeifidomniseryxopediuqilcisaB

0 2 81.1 edargHHKPhtiwdeifidomniseryxopediuqilcisaB

0 3.2 81.1 edargBHKPhtiwdeifidomnisercalovonyxopediuqiL

0 1.2 81.1 edargBHKPhtiwdeifidomNPEytisocsivwoL

0 2 01.1 dnelbyxonehP/yxopefonoisrepsidsuoeuqA

7 propyleneglycol n-propyl ether 8 dimethyl ethanolamine9 triethylamine

Reduced viscosity versions of InChemRez LER-HB with epoxy diluents available on request

INCHEMREZ NOTES

10

ytisocsiV 1 Pc,571ta oC

tnecrePyxonehP

,roloCrendraG EPW lacisyhP

mroF,gT oC

)CSD(

lacipyt lacipyt .ceps .ceps noitacificeps lacipyt

01-RES 0054 01 .xam2 568-577 elunarg/ekalf 05

P01-RES 0054 01 .xam2 568-577 redwop 05

52-RES 0081 2 52 .xam2 525-574 elunarg/ekalf 03<

ytisocsiV 3 Pc,52ta oC

sdiloS 4,%.tw

roloC 3,AHPA

ezaH 3,%

lacisyhPmroF

lyxordyHrebmun

).clac(

lacipyt noitacificeps .ceps .ceps noitacificeps lacipyt

08-PCKP 021 .nim79 .xam002 .xam51 stellep 061-551

76-PCKP 011 .nim79 .xam002 .xam51 dilos-imes 531-031

Pc,ytisocsiV52ta oC

,sdiloS%.tW

,roloCrendraG

tnelaviuqEthgiew

)sdilosno(mroFlacisyhP cificepS

ytivarG

lacipyt lacipyt .ceps lacipyt noitacificeps lacipyt

697-PE 000,64 06 .xam2 0012 diuqilsuocsiv 40.1

53-SE 000,6 53 .nim1 A/N diuqilsuocsiv A/N

05-SE .nim000,53 05 .xam2 0053 diuqilsuocsiv 30.1

56-RP 0002 07 .xam5 061 diuqilytisocsivwol 0.1

SOLID EPOXY/PHENOXY BLENDS

CAPROLACTONE-MODIFIED PHENOXY RESINS

EPOXY RESIN SOLUTIONS & CROSSLINKERS

1 ICI cone/plate 2 ICI cone/plate at 200oC

3 20% solution in cyclohexanone 4 gravimetric, 2 hours at 200oC

11

Pc,ytisocsiV041ta oC stnemmoC

lacipyt

000,11 sgnitaocredwopevitaroceddnalanoitcnufroF

000,11 foedargdezinorciM 01-RESzeRmehCnI

----- yollaniseryxopetnetnocyxonehPhgiH

,gT o ,C)CSD( stnemmoC

lacipyt

03 niseryxonehPdetfarg-enotcalorpacgTwol-muideM

2 yxonehPdetfarg-enotcalorpacgTwoL

tnevloS stnemmoC

noitacificeps

BE 5 KEMdna noitulosnidnelbyxonehP/yxopethgiewralucelomhgiH

AMPdnaKEM 6 noitulosnidnelbyxope/yxonehPthgiewralucelomhgiH

001-AdnaBE 7 noitulosniseryxopethgiewralucelomhgiH

lonatub-n slemanegnikabrofnisercilonehP

Caprolactone-modified Phenoxy resins have pendant branches with terminalprimary hydroxyls resulting from random grafting of e-caprolactone monomeronto the Phenoxy backbone. The esterification also results in lower glasstransition temperatures and lower product viscosities. (See page 12)

INCHEMREZ NOTES

5 ethyleneglycol butylether 6 propyleneglycol n-propylether acetate 7 Aromatic 100 solvent

12

Pc,ytisocsiV52ta oC

yxonehP%.tw EPW ,sdiloS

%.tw mroFlacisyhP ,roloCrendraG

lacipyt lacipyt .ceps .ceps noitacificeps .ceps

BH-REC 000,51-000,8 01 951-541 .nim99 diuqilsuocsiv .xam2

76PC-REC 008,4 01 951-541 .nim79 diuqilsuocsiv.dem .xam2

CYCLOALIPHATIC EPOXY /PHENOXY RESIN BLENDS

The PKCP-series of caprolactone modified Phenoxy resin are structurally represented below and modeled on page13. The random branches (typically x is about 2) produce resins with lower glass transitions than unmodified Phe-noxy, and enhance the compatibility with alkyl esters and polyesters.

INCHEMREZ NOTES

PHENOXY PKCP-series STRUCTURE

Phenoxy with e-Caprolactone Side Chain Grafting

13

ytilanoitcnuF)remogilO(

cificepSytivarG

HOrebmun stnemmoC

lacipyt lacipyt lacipyt

2 81.1 02 sniseryxonehPdnayxopecitahpilaolcycfodnelB

2 71.1 31 dnelbyxonehPdeifidom-enotcalorpac/yxopecitahpilaolcyC

The structural models below illustrate the comb-like structure of the caprolactone-modified Phenoxy resin whereinrandom secondary hydroxyls are converted to primary hydroxyls pendant on relatively short side chains comparedto the longer Phenoxy backbone

INCHEMREZ NOTES

CAPROLACTONE MODIFIED PHENOXY

14

The next sections of this guide show the diver-sity of applications of the InChemRez family ofproducts and the expected performance features& benefits that may be realized with their use incoatings, adhesives, plastics, and composites.Additionally, the many possible chemistries inwhich the InChemRez line can be incorporated issuggested.

HOW TO USE TABLES

The following tables are arranged in two fash-ions: product selections (in bold for best recom-mendation) are listed for performance attribute ver-sus application technology, followed by productselections for numerous chemical approaches ver-sus application technology.

The Phenoxy line of products find many usesas modifiers to other chemistries as well as utilityas the sole resinous vehicles in coatings, adhe-sives, etc. Compatibilty with urethanes and epoxyresins is excellent. In many cases modificationwith Phenoxy resin and its many derivatives issufficient to upgrade the properties of the formula-tion. In those cases where crosslinking can occurwith hydroxyl functionality the Phenoxy resins willfurther enhance properties like hardness, abrasionresistance, and chemical resistance.

SOLVENTS and DILUENTS

Phenoxy resins favor polar, aprotic type sol-vents in solventborne applications although incor-poration into formulations having hydrocarbon oraromatic solvents is quite possible if sufficient po-lar solvents can also be used. The preparation ofmost solventborne solutions of Phenoxy resins isusually straightforward given adequate agitation.For faster results some heating is required com-mensurate with the solvent choice.

APPLICATION GUIDELINES: Performance/Technology/Chemistry

WATERBORNE RESINS

Waterborne Phenoxy resins are colloidal dis-persions dependant on pH maintenance above 6.5.Generally they are compatible with colloidal dis-persions of other polmers stabilized in the samemanner such as polyurethanes, polyesters, acryl-ics, and epoxy esters. With waterborne epoxiespoor shelf stability is observed due to gellingtendencies of the contained epoxy species becauseof the slightly basic nature of the Phenoxydispersions.

TABLE SUMMARY

Coatings & Inks: pages 15 - 16Adhesives: pages 17 - 18Composites: pages 19 - 20Plastics: pages 21 - 22

TYPICAL PHENOXY APPLICATIONS

- Zinc-rich primers- Food & beverage can coatings- Maintenance coatings (metal & concrete)- Coil coatings- Marine coatings- Automotive refinish- Powder coatings- Cationic & UV cure- Tielayers- Heatseal adhesives- Structural adhesives

15

In coatings applications InChemRezPhenoxy resins, polyester modifiedPhenoxy resins, epoxy/Phenoxy hybridresins, and InChemRez caprolactonemodified resins offer a wide selectionfor your chosen technology. Phenoxyresins find use in can and container coat-ings, drum linings, zinc-rich coatings andmaintenance primers, shop primers, glassand plastic coatings, wood coatings, andcoatings for flexible substrates includingPET, metal foils, paper and cloth.

Water-borne grades of Phenoxy permitformulations to low VOC’s and select solidgrade Phenoxy resins are useful inthermoplastic and thermoset powdercoatings.

Solvent-borne

Water-borneair drythermoset

Powder

High Solids

serutaeFenrobtnevloS enrobretaW redwoP sdiloShgiH

noisehdAnoitomorp

HHKP04-SHKP

AMP03-SHKP

53-WHKP43-WHKPWBH-REL

08-PHKP001-BHKP

01-RES

76PC-REC52-RES

&ytilibixelFssenhguot

JHKP03-MHKP103-MHKP

52-RES

53-WHKP43-WHKP

08-PHKP001-BHKP

HH-REL

noisorroCecnatsiser

JHKP697-PE

53-WHKPWBH-REL

002-PHKP BH-RECBH-NEL

roloCwoL03-MHKP04-SHKP

43-WHKP 002-PHKP BH-REL

ssendraHEFKPJHKP

43-WHKPWBH-REL

01-RESP01-RES

BH-RECBH-NEL

ssolGAMP03-SHKP

HHKP43-WHKP 01-RES BH-REL

tnemgiPgnidaol

04-SHKPAMP03-SHKP

53-WHKP 001-BHKP08-PHKP

VLBH-NEL

Coatings & Inks Selection Guide

APPLICATION GUIDE: COATINGS FEATURE & TECHNOLOGY

16

yrtsimehCenrobtnevloS enrobretaW redwoP sdiloShgiH

enimA/yxopEtneibmaK2

HHKP04-SHKP

WBH-REL 76PC-RECBH-RECBH-NEL

VLBH-NEL

reknil-X/yxopEtnetalK1

002-PHKP001-BHKP

BH-RELBH-NEL

WBH-REL 08-PHKP001-BHKP

01-RES

BH-NELVLBH-NEL

OCN/retseyloPtneibmaK2

AMP03-SHKP103-MHKP

03-MHKP

63-WHKP43-WHKP

58-MHKP38-MHKP

OCN/retseyloPdekcolbK1

AMP03-SHKP103-MHKP

03-MHKP

43-WHKP63-WHKP

08-PHKP001-BHKP

76-PCKP58-MHKP38-MHKP

enimaleMtesomreht

HHKP04-SHKP103-MHKP

53-WHKP43-WHKP63-WHKP

08-PHKP001-BHKP

03-MHKP103-MHKP

58-MHKP

cilonehPtesomreht

HHKP04-SHKP

56-RP

53-WHKP43-WHKP

56-RP

01-RESP01-RES

03-MHKP103-MHKP

58-MHKP

yxopEcinoitaC

BH-REC76PC-REC

BH-REL

BH-REC76PC-REC

BH-NEL

enidirizAdeknilssorc

63-WHKP43-WHKP

/sdyklAsretseyxopE

43-WHKP63-WHKP

scilyrcA 43-WHKP63-WHKP

enahteruyloPsnoisrepsid

43-WHKP63-WHKP

/yxopEedirdyhna

BH-RELBH-NEL01-RES

BH-REC76PC-REC

InChemRez Phenoxy resins can be used as thesole resin vehicle in coatings formulations. Forcrosslinked systems using the pendant secondaryhydroxyls on the Phenoxy backbone it is recom-mended to empirically determine the best level ofcrosslinker for a balance of coatings properties such

as hardness and flexibility. Usually the level ofcrosslinker or hardener is about 10 to 15 phr (partsper hundred) on a solids basis. Typical crosslinkersused in thermoset applications are melamine-form-aldehyde resins, phenolics, blocked isocyanates,and polycarboxylic acids.

APPLICATION GUIDE: COATINGS CHEMISTRY TYPE & TECHNOLOGY

17

serutaeFenrobtnevloS enrobretaW tlemtoH sdiloshgiH

noisehdAnoitomorp

dilosllAsedargtellep

53-WHKP43-WHKPWBH-REL

dilosllAsedargtellep

76PC-RECBHKP

VLBH-NEL

&ytilibixelFssenhguot

JHKP03-MHKP103-MHKP

52-RES

53-WHKP43-WHKP EFKP

BH-REC

evisehoChtgnerts

JHKP697-PE

53-WHKP dilosllAsedargtellep

BHKP52-RES

taeHecnatsiser

EFKPJHKP

53-WHKP EFKP BH-REC

reirrabropaVseitreporp

dilosllAsedargtellep

53-WHKP dilosllAsedargtellep

BHKP

neerGhtgnerts

dilosllAsedargtellep

WBH-REL BHKP 01-RES

leePhtgnerts

EFKPJHKP

53-WHKP EFKPJHKP

52-RESVLBH-NEL

erutsioMecnatsiser

EFKP WBH-REL53-WHKP

dilosllAsedargtellep

HH-REL

Adhesives Selection Guide

Solventborne

Water-borneair drythermoset

Hot melt

High solidsthermosetair-dry 2k

In adhesives applications InChemRez Phenoxybased resins offer a wide selection for your chosentechnology.Phenoxy resins are used to add superior adhe-sion promotion to a wide variety of substrates. Thelarge number of secondary hydroxyls give Phenoxythe “bite” that many systems require. The linearthermoplastic nature of Phenoxy provides flexibil-ity to rigid crosslinked systems.Phenoxy resins find use in aerospace and auto-motive latent cure and hotmelt adhesives byimproving adhesion and flexibility of epoxy-basedcompounds, and circuit board laminating adhesivesby increasing bond strength to the boards.

APPLICATION GUIDE: ADHESIVES FEATURE & TECHNOLOGY

18

yrtsimehCenrobtnevloS enrobretaW tlemtoH sdiloShgiH

enimA/yxopEtneibmaK2

HHKP04-SHKP

WBH-REL 76PC-RECBH-RECBH-NEL

76PC-REC

reknil-X/yxopEtnetalK1

002-PHKP001-BHKP

BH-RELBH-NEL

WBH-REL 01-RES52-RES08-PHKP

BH-REL

BH-NEL

OCN/retseyloPtneibmaK2

AMP03-SHKP 63-WHKP 58-MHKP38-MHKP

OCN/retseyloPdekcolbK1

AMP03-SHKP 43-WHKP63-WHKP

103-MHKPBHKP

08-PCKP

76-PCKP58-MHKP38-MHKP

enimaleMtesomreht

HHKP04-SHKP

53-WHKP43-WHKP63-WHKP

03-MHKP103-MHKP

58-MHKP

cilonehPtesomreht

HHKP04-SHKP

56-RP

53-WHKP43-WHKP

56-RP

03-MHKP103-MHKP

58-MHKP

yxopEcinoitaC

BH-REC76PC-REC

BH-REL

BH-REC76PC-REC

BH-NEL

AVEtlemtoh

BHKP103-MHKP

08-PCKP

BHKP001-BHKP

08-PHKP

UPTtlemtoh

08-PHKP08-PCKP

BHKP

002-PHKPHHKPBHKP

InChemRez Phenoxy resins can be used as thesole resin vehicle in adhesives formulations. Forcrosslinked systems using the pendant second-ary hydroxyls on the Phenoxy backbone it is rec-ommended to empirically determine the best levelof crosslinker for a balance of coatings propertiessuch as hardness and flexibility. Usually the levelof crosslinker or hardener is about 10 to 15 phr(parts per hundred) on a solids basis. Typicalcrosslinkers used in thermoset applications aremelamine-formaldehyde resins, phenolics, blockedisocyanates, and polycarboxylic acids. InChemnow provides a phenolic crosslinker calledInChemRez PR-65 (see page 10) useful for ther-moset coatings and adhesives based on hydroxylfunctional vehicles like solid grade epoxies, OH-functional polyesters, and Phenoxy resins.

In hot melt applications with thermoplastic ure-thanes (TPU’s) and copolyethylene vinyl acetateresins (EVA’s) Phenoxy resins can be incorpor-

ated at levels as low as 10% to act as antiplastizersimparting properties such as stiffness and cohe-sive strength.

For modifying epoxy systems, the powder gradesof Phenoxy are easy to incorporate. Alternatively,the liquid and solid blends offered by InChem pro-vide a “user friendly” avenue. Phenoxy behaves asa “hard plasticizer” in many epoxy matrices usedas adhesives by interpenetration. In acid curedand anhydride-cured systems Phenoxy may par-tially tie into the cured matrix.

APPLICATION GUIDE: ADHESIVES CHEMISTRY TYPE & TECHNOLOGY

19

Solventborne

Water-borne

High solids

Composites Selection Guide

InChemRez Phenoxy resins havespecific uses in composites applica-tions both in fiber sizing and in matrixresin compostions. Phenoxy resinshave excellent adhesion to glass andcarbon fibers. Phenoxy sizings enableexellent compatibilty with epoxy-basedmatrix resins, and with viny ester basedresins.

Because of the pendant backbone hy-droxyls, Phenoxy can be thermosetwith select crosslinkers to provide maxi-mum strength, heat resistance, andchemical resistance.

Phenoxy can also be formulated intoepoxy and urethane based compositeformulations to provide toughness andadhesion to the reinforcement.

serutaeFenrobtnevloS enrobretaW sdiloshgiH

tuoteWdilosllA

sedargtellep53-WHKP43-WHKP

&ytilibixelFssenhguot

JHKP52-RES

53-WHKP43-WHKP

BH-RELVLBH-NEL

elisneThtgnerts

JHKPEFKP

53-WHKP BHKP52-RES

eruCdeeps

01-RESBH-REL

63-WHKP BH-REC58-MHKP

taeHecnatsiser

dilosllAsedargtellep

53-WHKP BHKP

scinoiwoLdilosllA

sedargtellep BH-NELVLBH-NEL

erutsioMecnatsiser

EFKP56-RP

53-WHKP BH-NEL

APPLICATION GUIDE: COMPOSITE FEATURE & TECHNOLOGY

20

yrtsimehCenrobtnevloS enrobretaW sdiloShgiH

enimA/yxopEtneibmaK2

HHKP04-SHKP

52-RES01-RES

WBH-REL VLBH-NELBH-RECBH-NEL52-RES

reknil-X/yxopEtnetalK1

002-PHKP52-RES01-RESBH-NEL

WBH-REL BH-NELVLBH-NEL

52-RES01-RES

OCN/retseyloPtneibmaK2

AMP03-SHKP 63-WHKP43-WHKP

58-MHKP38-MHKP

OCN/retseyloPdekcolbK1

AMP03-SHKP 43-WHKP63-WHKP

76-PCKP58-MHKP38-MHKP

etalyrcAerucedixorep

BHKP

cilonehPtesomreht

HHKP04-SHKP

56-RP

53-WHKP43-WHKP

56-RP

03-MHKP103-MHKP

58-MHKP

yxopEcinoitaC

BH-REC76PC-REC

BH-REL

BH-REC76PC-REC

BH-NEL

enimaleMtesomreht

HHKP04-SHKP76-PCKP

43-WHKP53-WHKP

BHKP001-BHKP

08-PHKP

APPLICATION GUIDE: COMPOSITE CHEMISTRY TYPE & TECHNOLOGY

21

Plastics Selection Guide

In plastics applications InChemRezPhenoxy resins offer a wide selection foryour chosen technology. Phenoxy resinsfind use in blends of PBT, PET, PPO,nylon, and polycarbonate resins for modi-fying physical properties such as tensile,flexural, and impact strengths. The additionof Phenoxy improves pigment/filler wettingfor appearance and rheology control.Additionally Phenoxy resins are useful ascompatibilizing agents for dissimilarplastics like polyolefins and polyesters.

Because of transesterification reactionsPhenoxy resin can behave as processingaids with polyesters such as polyethyleneterephthalate during extrusion.

Processing Aid

Blends

Compatibilizer

Tie-layer

serutaeFdiAgnissecorP sdnelB rezilibitapmoC reyal-eiT

elisneThtgnerts

dilosllAsedargtellep

EFKP HHKP HHKPJHKP

elisneTsuludom

JHKPEFKP

EFKPJHKP

HHKP JHKPEFKP

laruxelFhtgnerts

JHKP EFKP HHKPEFKP

EFKP

laruxelFsuludom

EFKP EFKP HHKPJHKP

JHKPEFKP

tcapmIhtgnerts

EFKP EFKP08-PCKP

BHKPEFKP

HHKP

tnemgiPgnittew

dilosllAsedargtellep

EFKP HHKPEFKP

ytiralCrolocdna

HHKP HHKPHHKP HHKP

ropaVreirrab

dilosllAsedargtellep

EFKPHHKP EFKP

HHKP

APPLICATION GUIDE: PLASTICS FEATURE & TECHNOLOGY

22

yrtsimehCdiAgnissecorP sdnelB rezilibitapmoC reyal-eiT

TEP/TBPHHKPEFKP

BHKPEFKP

BHKPEFKP

HHKP

-lynehpyloPedixoene

HHKPEFKP

EFKP EFKP HHKP

nolyNEFKP EFKP EFKP EFKP

HHKP

etanobracyloPEFKP EFKP HHKP

snifeloyloPEFKP

-lynivyloPlarytub

EFKPEFKPHHKP

lynivyloPenodilorryp

EFKPHHKPBHKP

s'UPT HHKPEFKP

HHKPCHKPBHKP

enelyklayloPsedixo

EFKPHHKP

HHKP

-orpacyloPenotcal

HHKPEFKP EFKP

HHKP HHKPHHKP

Because of its unique structure and propertiesPhenoxy resins, when used as additives in plas-tics applications, can greatly improve not only theprocessability of these materials but also improvethe quality and performance of the finishedproduct.

During processing the addition of Phenoxy canhelp to control process rheology as well as the heatdistortion temperatures in extrusion, molding andfilm formation operations. The amorphous nature ofPhenoxy resin can also be helpful in controllingthe crystallization kinetics of thermoplasticmaterials.

Alloys made with Phenoxy have been shown topossess improved thermal stability. The tough-ness of Phenoxy resins also imparts improvedmechanical performance to finished products. Asa result, the addition of Phenoxy resins can re-sult in cost reductions as less material (thinnercross sections) is required to achieve the desiredperformance. The excellect vapor barrier proper-ties of Phenoxy resins can be beneficial in plasticfilm applications where protection against mois-ture or oxygen is required.

APPLICATION GUIDE: PLASTIC CHEMISTRY TYPE & TECHNOLOGY

23

VISCOSITY PROFILES FOR PHENOXY RESINS IN CYCLOHEXANONE AND METHYL ETHYL KETONE

10

100

1000

10000

100000

1000000

10000000

0 10 20 30 40 50

Percent solids

Visc

osity

, cP

at 2

5o C

PKHB

PKHJ

PKHH

Cyclohexanone

Methyl ethyl ketone

Viscosity/solids relationships for standard grades of Phenoxyresins in common solvents and solvent mixtures are shownon pages 23-25. On page 26 a list of common solvents anddiluents for standard Phenoxy resin is tabulated. Wherenoted, the solubility of Phenoxy resins may be limited, es-pecially in situations where the solvent is in high excess (lowsolids region). For example, with methyl ethyl ketone, phaseout will occur with Phenoxy resin (PKHH, PKHB) below about22% solids. Interestingly, the phase out can be rectified witha small addition of water (about 1%).

24

VISCOSITY PROFILES FOR PHENOXY RESINS IN BINARY SOLVENT BLEND: MEK AND AROMATIC 100

10

100

1000

10000

100000

0 10 20 30 40 50

Percent Solids

Visc

osity

, in

cP a

t 25o C

PKHB

SOLVENT BLEND IS: 3:2 by weight MEK Aromatic 100 PKHH

VISCOSITY PROFILES FOR PHENOXY RESINS IN PM SOLVENT AND PM ACETATE

10

100

1000

10000

100000

1000000

0 5 10 15 20 25 30 35 40 45

Percent Solids

Visc

osity

, cP

at 2

5o C

PM Acetate

PM Solvent

PKHJ

PKHH

PKHB

25

VISCOSITY PROFILES FOR PHENOXY RESINS IN LOW VOC TERNARY SOLVENT BLENDS

10

100

1000

10000

100000

0 10 20 30 40 50 60

Percent Solids

Visc

osity

, in

cP a

t 25o C

SOLVENT BLEND IS: 1:1:1 by weight cyclohexanone acetone (VOC exempt) methyl acetate (VOC exempt)

PKHH

PKHB

VISCOSITY PROFILES FOR PHENOXY RESINS IN PM ACETATE/AROMATIC 100 (3/2)

1000

10000

100000

1000000

0 10 20 30 40 50 60

Percent Solids

Visc

osity

, in

cP a

t 25o C

PKHH

PKHB

Insoluble mixtures below this pointat 25oC

Weight ratio of PM Acetateto Aromatic 100 solventsis 3 parts to 2 parts

26

Phenoxy Resin CommentsSolubility

Solvent Type:

Ketones:cyclohexanone Excellent

methy ethyl ketone (MEK) Good Phase separation below 22% solidsmethyl isobutyl ketone (MIBK) Insoluble (at 25% NV)

methyl amyl ketone (MAK) Insoluble (at 25% NV)acetone Insoluble (at 25% NV) Soluble at > 45% NV

Alcohols:methanol, ethanol, butanol Insoluble

isopropanol Insolublebenzyl alcohol Good

Glycol ethers:ethyleneglycol alkyl ethers Excellent Cellosolve, butyl Cellosolve, etc. (Dow)

diethyleneglycol alkyl ethers Excellent Carbitol, butyl Carbitol, etc. (Dow)propyleneglycol alkyl ethers Excellent

dipropyleneglycol al kyl ethers Excellentphenoxypropanol Excellent Dowanol PPh (Dow)

Esters:alkyl acetates Insoluble methyl , or ethyl , or butyl acetate, etc.

ethyl lactate Gooddibasic esters Good DBE (DuPont)

ethyleneglycol ethylether acetate Gooddiethyleneglycol ethylether acetate Good

propyleneglycol methylether acetate Goodethoxyethyl propionate Good Ektapro EEP (Eastman)phenoxyethyl acrylate Good

tripropyleneglycol diacrylate Goodhexanediol diacrylate Poor

Hydrocarbons:toluene Insoluble These materials are useful diluentsxylene Insoluble for Phenoxy when combined with

Aromatic 100 Insoluble polar, aprotic solvents; use at 40%hexane Insoluble maximum on solvent basis

Miscellaneous:tetrahydrofuran Excellent

N-methyl pyrrolidone Excellentp-chloro benzotrifluoride Insoluble

diacetone alcohol Goodcresyl glycidylether Goodbutyl glycidylether Insoluble

methylene chloride Good

PHENOXY SOLVENT TABLE

lacirtcelE/lamrehT/lacinahceM retemaraP ygolodohteMtseT

bl-tf,tcapmIdozIdehctoN 5.2 )MTSA(652D

37ta,.ni/bl-tf,tcapmIyprahC oF kaerboN 652D

04-ta oF kaerboN

etamitlu,isp,htgnertSelisneT 0059 836D

dleiyta 0009

etamitlu,%,noitagnolE 09 836D

dleiyta 5.3

noisnetni,isp,suludomcitsalE 000,083 836D

eruxelfni 000,014 097D

isp,htgnertslaruxelF ).ni0.5x.ni5.0x.ni52.0( 000,41 097D

,isp,ssertsdleiyevisserpmoC )1x1x1( 596D

noitcelfed%1 0072

dleiymumixaM 000,21

suludoM 000,523

%,dleiytaniartS 9

oitars'nossioP 83.0

,erutarepmetnoitrotsidtaeH o isp462ta,F 4.881 846D

/.ni/.ni,ECT o 22-rof,F o 68otF oF 01x2.3 5-

68rof o 041otF oF 01x8.3 5-

mc-mho,ytivitsiseremuloV 01x5> 31 752D

ztrehagem1,tnatsnoccirtceleiD 8.3 051D

ztrehagem1,rotcafnoitapassiD 30.0 051D

77ta,xednievitcarfeR oF 8795.1

elacsR,ssendrahllewkcoR 321 587D

37taseulavlla[ o ]esiwrehtodetatssselnu,F

PROPERTIES OF INCHEMREZ PHENOXY PKFE SOLID GRADE


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