GB1304927A

GB1304927A – – Google Patents

GB1304927A – – Google Patents

Info

Publication number
GB1304927A

GB1304927A
GB1209670A
GB1209670A
GB1304927A
GB 1304927 A
GB1304927 A
GB 1304927A
GB 1209670 A
GB1209670 A
GB 1209670A
GB 1209670 A
GB1209670 A
GB 1209670A
GB 1304927 A
GB1304927 A
GB 1304927A
Authority
GB
United Kingdom
Prior art keywords
ethyl
rubber
benzaldehyde
butyl
tetra
Prior art date
1969-03-17
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired

Application number
GB1209670A
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
1969-03-17
Filing date
1970-03-13
Publication date
1973-01-31

1970-03-13
Application filed
filed
Critical

1973-01-31
Publication of GB1304927A
publication
Critical
patent/GB1304927A/en

Status
Expired
legal-status
Critical
Current

Links

Espacenet

Global Dossier

Discuss

-1
verataldehyde
Chemical compound

0.000
abstract
7

229920001971
elastomer
Polymers

0.000
abstract
6

239000005060
rubber
Substances

0.000
abstract
6

239000000203
mixture
Substances

0.000
abstract
5

239000000126
substance
Substances

0.000
abstract
4

239000004753
textile
Substances

0.000
abstract
4

150000001412
amines
Chemical class

0.000
abstract
3

HUMNYLRZRPPJDN-UHFFFAOYSA-N
benzenecarboxaldehyde
Natural products

O=CC1=CC=CC=C1
HUMNYLRZRPPJDN-UHFFFAOYSA-N
0.000
abstract
3

229920000728
polyester
Polymers

0.000
abstract
3

DSSYKIVIOFKYAU-OIBJUYFYSA-N
(S)-camphor
Chemical compound

C1C[C@]2(C)C(=O)C[C@H]1C2(C)C
DSSYKIVIOFKYAU-OIBJUYFYSA-N
0.000
abstract
2

VXNZUUAINFGPBY-UHFFFAOYSA-N
1-Butene
Chemical compound

CCC=C
VXNZUUAINFGPBY-UHFFFAOYSA-N
0.000
abstract
2

JIVGSHFYXPRRSZ-UHFFFAOYSA-N
2,3-dimethoxybenzaldehyde
Chemical compound

COC1=CC=CC(C=O)=C1OC
JIVGSHFYXPRRSZ-UHFFFAOYSA-N
0.000
abstract
2

IUNJCFABHJZSKB-UHFFFAOYSA-N
2,4-dihydroxybenzaldehyde
Chemical compound

OC1=CC=C(C=O)C(O)=C1
IUNJCFABHJZSKB-UHFFFAOYSA-N
0.000
abstract
2

LWRSYTXEQUUTKW-UHFFFAOYSA-N
2,4-dimethoxybenzaldehyde
Chemical compound

COC1=CC=C(C=O)C(OC)=C1
LWRSYTXEQUUTKW-UHFFFAOYSA-N
0.000
abstract
2

YEJRWHAVMIAJKC-UHFFFAOYSA-N
4-Butyrolactone
Chemical compound

O=C1CCCO1
YEJRWHAVMIAJKC-UHFFFAOYSA-N
0.000
abstract
2

RGHHSNMVTDWUBI-UHFFFAOYSA-N
4-hydroxybenzaldehyde
Chemical compound

OC1=CC=C(C=O)C=C1
RGHHSNMVTDWUBI-UHFFFAOYSA-N
0.000
abstract
2

FZHSPPYCNDYIKD-UHFFFAOYSA-N
5-methoxysalicylaldehyde
Chemical compound

COC1=CC=C(O)C(C=O)=C1
FZHSPPYCNDYIKD-UHFFFAOYSA-N
0.000
abstract
2

PPBRXRYQALVLMV-UHFFFAOYSA-N
Styrene
Chemical compound

C=CC1=CC=CC=C1
PPBRXRYQALVLMV-UHFFFAOYSA-N
0.000
abstract
2

150000008064
anhydrides
Chemical class

0.000
abstract
2

ISAOCJYIOMOJEB-UHFFFAOYSA-N
benzoin
Chemical compound

C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1
ISAOCJYIOMOJEB-UHFFFAOYSA-N
0.000
abstract
2

XUPYJHCZDLZNFP-UHFFFAOYSA-N
butyl butanoate
Chemical compound

CCCCOC(=O)CCC
XUPYJHCZDLZNFP-UHFFFAOYSA-N
0.000
abstract
2

229920001577
copolymer
Polymers

0.000
abstract
2

WTWBUQJHJGUZCY-UHFFFAOYSA-N
cuminaldehyde
Chemical compound

CC(C)C1=CC=C(C=O)C=C1
WTWBUQJHJGUZCY-UHFFFAOYSA-N
0.000
abstract
2

230000006866
deterioration
Effects

0.000
abstract
2

150000001993
dienes
Chemical class

0.000
abstract
2

WOZVHXUHUFLZGK-UHFFFAOYSA-N
dimethyl terephthalate
Chemical compound

COC(=O)C1=CC=C(C(=O)OC)C=C1
WOZVHXUHUFLZGK-UHFFFAOYSA-N
0.000
abstract
2

HYBBIBNJHNGZAN-UHFFFAOYSA-N
furfural
Chemical compound

O=CC1=CC=CO1
HYBBIBNJHNGZAN-UHFFFAOYSA-N
0.000
abstract
2

OSWPMRLSEDHDFF-UHFFFAOYSA-N
methyl salicylate
Chemical compound

COC(=O)C1=CC=CC=C1O
OSWPMRLSEDHDFF-UHFFFAOYSA-N
0.000
abstract
2

QNGNSVIICDLXHT-UHFFFAOYSA-N
para-ethylbenzaldehyde
Natural products

CCC1=CC=C(C=O)C=C1
QNGNSVIICDLXHT-UHFFFAOYSA-N
0.000
abstract
2

QKFJKGMPGYROCL-UHFFFAOYSA-N
phenyl isothiocyanate
Chemical compound

S=C=NC1=CC=CC=C1
QKFJKGMPGYROCL-UHFFFAOYSA-N
0.000
abstract
2

SMQUZDBALVYZAC-UHFFFAOYSA-N
salicylaldehyde
Chemical compound

OC1=CC=CC=C1C=O
SMQUZDBALVYZAC-UHFFFAOYSA-N
0.000
abstract
2

URAYPUMNDPQOKB-UHFFFAOYSA-N
triacetin
Chemical compound

CC(=O)OCC(OC(C)=O)COC(C)=O
URAYPUMNDPQOKB-UHFFFAOYSA-N
0.000
abstract
2

RRKODOZNUZCUBN-CCAGOZQPSA-N
(1z,3z)-cycloocta-1,3-diene
Chemical compound

C1CC\C=C/C=C\C1
RRKODOZNUZCUBN-CCAGOZQPSA-N
0.000
abstract
1

IZPOFBCRCRPFLW-UHFFFAOYSA-N
(3-hydroxy-2-methyl-2-nitropropyl) hydrogen sulfite
Chemical compound

S(=O)(O)OCC(CO)(C)[N+](=O)[O-]
IZPOFBCRCRPFLW-UHFFFAOYSA-N
0.000
abstract
1

PRBHEGAFLDMLAL-GQCTYLIASA-N
(4e)-hexa-1,4-diene
Chemical compound

C\C=C\CC=C
PRBHEGAFLDMLAL-GQCTYLIASA-N
0.000
abstract
1

OJOWICOBYCXEKR-KRXBUXKQSA-N
(5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene
Chemical compound

C1C2C(=C/C)/CC1C=C2
OJOWICOBYCXEKR-KRXBUXKQSA-N
0.000
abstract
1

KJPRLNWUNMBNBZ-QPJJXVBHSA-N
(E)-cinnamaldehyde
Chemical compound

O=C\C=C\C1=CC=CC=C1
KJPRLNWUNMBNBZ-QPJJXVBHSA-N
0.000
abstract
1

XEMRAKSQROQPBR-UHFFFAOYSA-N
(trichloromethyl)benzene
Chemical compound

ClC(Cl)(Cl)C1=CC=CC=C1
XEMRAKSQROQPBR-UHFFFAOYSA-N
0.000
abstract
1

AGYUOJIYYGGHKV-UHFFFAOYSA-N
1,2-bis(2-chloroethoxy)ethane
Chemical compound

ClCCOCCOCCCl
AGYUOJIYYGGHKV-UHFFFAOYSA-N
0.000
abstract
1

VGHSXKTVMPXHNG-UHFFFAOYSA-N
1,3-diisocyanatobenzene
Chemical compound

O=C=NC1=CC=CC(N=C=O)=C1
VGHSXKTVMPXHNG-UHFFFAOYSA-N
0.000
abstract
1

ZZHIDJWUJRKHGX-UHFFFAOYSA-N
1,4-bis(chloromethyl)benzene
Chemical compound

ClCC1=CC=C(CCl)C=C1
ZZHIDJWUJRKHGX-UHFFFAOYSA-N
0.000
abstract
1

OTEKOJQFKOIXMU-UHFFFAOYSA-N
1,4-bis(trichloromethyl)benzene
Chemical compound

ClC(Cl)(Cl)C1=CC=C(C(Cl)(Cl)Cl)C=C1
OTEKOJQFKOIXMU-UHFFFAOYSA-N
0.000
abstract
1

VSFHYKIILWBKOH-UHFFFAOYSA-N
2,2-dimethylocta-3,4-dienal
Chemical compound

CCCC=C=CC(C)(C)C=O
VSFHYKIILWBKOH-UHFFFAOYSA-N
0.000
abstract
1

GOXQRTZXKQZDDN-UHFFFAOYSA-N
2-Ethylhexyl acrylate
Chemical compound

CCCCC(CC)COC(=O)C=C
GOXQRTZXKQZDDN-UHFFFAOYSA-N
0.000
abstract
1

XAONNFGJDVVIIN-UHFFFAOYSA-N
3,3-dimethylhexane-2,4-dione
Chemical compound

CCC(=O)C(C)(C)C(C)=O
XAONNFGJDVVIIN-UHFFFAOYSA-N
0.000
abstract
1

QPGLMFYXCFKPSF-UHFFFAOYSA-N
3,5,5-trimethyl-2H-pyran-6-one
Chemical compound

CC1(C(=O)OCC(=C1)C)C
QPGLMFYXCFKPSF-UHFFFAOYSA-N
0.000
abstract
1

ZDYXJTFVVBRTCV-UHFFFAOYSA-N
3-(chloromethyl)-2-hydroxybenzaldehyde
Chemical compound

OC1=C(CCl)C=CC=C1C=O
ZDYXJTFVVBRTCV-UHFFFAOYSA-N
0.000
abstract
1

JEQMCLSTBFLNCO-UHFFFAOYSA-N
3-(chloromethyl)-5-hydroxybenzaldehyde
Chemical compound

ClCC=1C=C(C=O)C=C(C1)O
JEQMCLSTBFLNCO-UHFFFAOYSA-N
0.000
abstract
1

KAYAKFYASWYOEB-UHFFFAOYSA-N
3-octadec-1-enyloxolane-2,5-dione
Chemical compound

CCCCCCCCCCCCCCCCC=CC1CC(=O)OC1=O
KAYAKFYASWYOEB-UHFFFAOYSA-N
0.000
abstract
1

UFERIGCCDYCZLN-UHFFFAOYSA-N
3a,4,7,7a-tetrahydro-1h-indene
Chemical compound

C1C=CCC2CC=CC21
UFERIGCCDYCZLN-UHFFFAOYSA-N
0.000
abstract
1

OECTYKWYRCHAKR-UHFFFAOYSA-N
4-vinylcyclohexene dioxide
Chemical compound

C1OC1C1CC2OC2CC1
OECTYKWYRCHAKR-UHFFFAOYSA-N
0.000
abstract
1

PSBKJPTZCVYXSD-UHFFFAOYSA-N
5-methylheptan-3-one
Chemical compound

CCC(C)CC(=O)CC
PSBKJPTZCVYXSD-UHFFFAOYSA-N
0.000
abstract
1

NLHHRLWOUZZQLW-UHFFFAOYSA-N
Acrylonitrile
Chemical compound

C=CC#N
NLHHRLWOUZZQLW-UHFFFAOYSA-N
0.000
abstract
1

MRABAEUHTLLEML-UHFFFAOYSA-N
Butyl lactate
Chemical compound

CCCCOC(=O)C(C)O
MRABAEUHTLLEML-UHFFFAOYSA-N
0.000
abstract
1

239000004287
Dehydroacetic acid
Substances

0.000
abstract
1

DKMROQRQHGEIOW-UHFFFAOYSA-N
Diethyl succinate
Chemical compound

CCOC(=O)CCC(=O)OCC
DKMROQRQHGEIOW-UHFFFAOYSA-N
0.000
abstract
1

JIGUQPWFLRLWPJ-UHFFFAOYSA-N
Ethyl acrylate
Chemical compound

CCOC(=O)C=C
JIGUQPWFLRLWPJ-UHFFFAOYSA-N
0.000
abstract
1

239000004606
Fillers/Extenders
Substances

0.000
abstract
1

VQTUBCCKSQIDNK-UHFFFAOYSA-N
Isobutene
Chemical group

CC(C)=C
VQTUBCCKSQIDNK-UHFFFAOYSA-N
0.000
abstract
1

239000005062
Polybutadiene
Substances

0.000
abstract
1

229920002472
Starch
Polymers

0.000
abstract
1

244000028419
Styrax benzoin
Species

0.000
abstract
1

235000000126
Styrax benzoin
Nutrition

0.000
abstract
1

AWMVMTVKBNGEAK-UHFFFAOYSA-N
Styrene oxide
Chemical compound

C1OC1C1=CC=CC=C1
AWMVMTVKBNGEAK-UHFFFAOYSA-N
0.000
abstract
1

235000008411
Sumatra benzointree
Nutrition

0.000
abstract
1

BOTDANWDWHJENH-UHFFFAOYSA-N
Tetraethyl orthosilicate
Chemical compound

CCO[Si](OCC)(OCC)OCC
BOTDANWDWHJENH-UHFFFAOYSA-N
0.000
abstract
1

AXMVYSVVTMKQSL-UHFFFAOYSA-N
UNPD142122
Natural products

OC1=CC=C(C=CC=O)C=C1O
AXMVYSVVTMKQSL-UHFFFAOYSA-N
0.000
abstract
1

239000012190
activator
Substances

0.000
abstract
1

239000000853
adhesive
Substances

0.000
abstract
1

230000001070
adhesive effect
Effects

0.000
abstract
1

MMCPOSDMTGQNKG-UJZMCJRSSA-N
aniline;hydrochloride
Chemical compound

Cl.N[14C]1=[14CH][14CH]=[14CH][14CH]=[14CH]1
MMCPOSDMTGQNKG-UJZMCJRSSA-N
0.000
abstract
1

239000003963
antioxidant agent
Substances

0.000
abstract
1

HUMNYLRZRPPJDN-KWCOIAHCSA-N
benzaldehyde
Chemical group

O=[11CH]C1=CC=CC=C1
HUMNYLRZRPPJDN-KWCOIAHCSA-N
0.000
abstract
1

WURBFLDFSFBTLW-UHFFFAOYSA-N
benzil
Chemical compound

C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1
WURBFLDFSFBTLW-UHFFFAOYSA-N
0.000
abstract
1

229960002130
benzoin
Drugs

0.000
abstract
1

KCXMKQUNVWSEMD-UHFFFAOYSA-N
benzyl chloride
Chemical compound

ClCC1=CC=CC=C1
KCXMKQUNVWSEMD-UHFFFAOYSA-N
0.000
abstract
1

229940073608
benzyl chloride
Drugs

0.000
abstract
1

239000001191
butyl (2R)-2-hydroxypropanoate
Substances

0.000
abstract
1

ZAZUOXBHFXAWMD-UHFFFAOYSA-N
butyl 2-oxopropanoate
Chemical compound

CCCCOC(=O)C(C)=O
ZAZUOXBHFXAWMD-UHFFFAOYSA-N
0.000
abstract
1

229930188620
butyrolactone
Natural products

0.000
abstract
1

239000003795
chemical substances by application
Substances

0.000
abstract
1

229940117916
cinnamic aldehyde
Drugs

0.000
abstract
1

KJPRLNWUNMBNBZ-UHFFFAOYSA-N
cinnamic aldehyde
Natural products

O=CC=CC1=CC=CC=C1
KJPRLNWUNMBNBZ-UHFFFAOYSA-N
0.000
abstract
1

239000002131
composite material
Substances

0.000
abstract
1

238000010276
construction
Methods

0.000
abstract
1

125000004122
cyclic group
Chemical group

0.000
abstract
1

HJSLFCCWAKVHIW-UHFFFAOYSA-N
cyclohexane-1,3-dione
Chemical compound

O=C1CCCC(=O)C1
HJSLFCCWAKVHIW-UHFFFAOYSA-N
0.000
abstract
1

JEQRBTDTEKWZBW-UHFFFAOYSA-N
dehydroacetic acid
Chemical compound

CC(=O)C1=C(O)OC(C)=CC1=O
JEQRBTDTEKWZBW-UHFFFAOYSA-N
0.000
abstract
1

229940061632
dehydroacetic acid
Drugs

0.000
abstract
1

PGRHXDWITVMQBC-UHFFFAOYSA-N
dehydroacetic acid
Natural products

CC(=O)C1C(=O)OC(C)=CC1=O
PGRHXDWITVMQBC-UHFFFAOYSA-N
0.000
abstract
1

235000019258
dehydroacetic acid
Nutrition

0.000
abstract
1

KSKWGMNRWCYVAT-UHFFFAOYSA-N
diethyl 2,5-dioxocyclohexane-1,4-dicarboxylate
Chemical compound

CCOC(=O)C1CC(=O)C(C(=O)OCC)CC1=O
KSKWGMNRWCYVAT-UHFFFAOYSA-N
0.000
abstract
1

BADXJIPKFRBFOT-UHFFFAOYSA-N
dimedone
Chemical compound

CC1(C)CC(=O)CC(=O)C1
BADXJIPKFRBFOT-UHFFFAOYSA-N
0.000
abstract
1

238000007598
dipping method
Methods

0.000
abstract
1

125000005066
dodecenyl group
Chemical group

C(=CCCCCCCCCCC)*

0.000
abstract
1

230000000694
effects
Effects

0.000
abstract
1

239000003822
epoxy resin
Substances

0.000
abstract
1

150000002148
esters
Chemical class

0.000
abstract
1

FWDBOZPQNFPOLF-UHFFFAOYSA-N
ethenyl(triethoxy)silane
Chemical compound

CCO[Si](OCC)(OCC)C=C
FWDBOZPQNFPOLF-UHFFFAOYSA-N
0.000
abstract
1

VRZVPALEJCLXPR-UHFFFAOYSA-N
ethyl 4-methylbenzenesulfonate
Chemical compound

CCOS(=O)(=O)C1=CC=C(C)C=C1
VRZVPALEJCLXPR-UHFFFAOYSA-N
0.000
abstract
1

239000004744
fabric
Substances

0.000
abstract
1

239000000835
fiber
Substances

0.000
abstract
1

239000000945
filler
Substances

0.000
abstract
1

235000013773
glyceryl triacetate
Nutrition

0.000
abstract
1

239000001087
glyceryl triacetate
Substances

0.000
abstract
1

235000019382
gum benzoic
Nutrition

0.000
abstract
1

LNEPOXFFQSENCJ-UHFFFAOYSA-N
haloperidol
Chemical compound

C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1
LNEPOXFFQSENCJ-UHFFFAOYSA-N
0.000
abstract
1

JJTUDXZGHPGLLC-UHFFFAOYSA-N
lactide
Chemical compound

CC1OC(=O)C(C)OC1=O
JJTUDXZGHPGLLC-UHFFFAOYSA-N
0.000
abstract
1

229920000126
latex
Polymers

0.000
abstract
1

239000000314
lubricant
Substances

0.000
abstract
1

229960001047
methyl salicylate
Drugs

0.000
abstract
1

CQDGTJPVBWZJAZ-UHFFFAOYSA-N
monoethyl carbonate
Chemical compound

CCOC(O)=O
CQDGTJPVBWZJAZ-UHFFFAOYSA-N
0.000
abstract
1

229920003052
natural elastomer
Polymers

0.000
abstract
1

229920001194
natural rubber
Polymers

0.000
abstract
1

150000003891
oxalate salts
Chemical class

0.000
abstract
1

238000010422
painting
Methods

0.000
abstract
1

PNJWIWWMYCMZRO-UHFFFAOYSA-N
pent‐4‐en‐2‐one
Natural products

CC(=O)CC=C
PNJWIWWMYCMZRO-UHFFFAOYSA-N
0.000
abstract
1

229940117953
phenylisothiocyanate
Drugs

0.000
abstract
1

239000000049
pigment
Substances

0.000
abstract
1

229920001084
poly(chloroprene)
Polymers

0.000
abstract
1

229920005735
poly(methyl vinyl ketone)
Polymers

0.000
abstract
1

229920002857
polybutadiene
Polymers

0.000
abstract
1

150000004291
polyenes
Chemical class

0.000
abstract
1

229920000647
polyepoxide
Polymers

0.000
abstract
1

229920001195
polyisoprene
Polymers

0.000
abstract
1

229920000642
polymer
Polymers

0.000
abstract
1

229920002689
polyvinyl acetate
Polymers

0.000
abstract
1

239000011118
polyvinyl acetate
Substances

0.000
abstract
1

ADPUQRRLAAPXGT-UHFFFAOYSA-M
sodium;2-formylbenzenesulfonate
Chemical compound

[Na+].[O-]S(=O)(=O)C1=CC=CC=C1C=O
ADPUQRRLAAPXGT-UHFFFAOYSA-M
0.000
abstract
1

238000005507
spraying
Methods

0.000
abstract
1

238000003892
spreading
Methods

0.000
abstract
1

239000008107
starch
Substances

0.000
abstract
1

235000019698
starch
Nutrition

0.000
abstract
1

229920003051
synthetic elastomer
Polymers

0.000
abstract
1

239000005061
synthetic rubber
Substances

0.000
abstract
1

KUCOHFSKRZZVRO-UHFFFAOYSA-N
terephthalaldehyde
Chemical compound

O=CC1=CC=C(C=O)C=C1
KUCOHFSKRZZVRO-UHFFFAOYSA-N
0.000
abstract
1

SWQWONXMUXCEDF-UHFFFAOYSA-N
tetrakis(2-ethylbutyl) silicate
Chemical compound

CCC(CC)CO[Si](OCC(CC)CC)(OCC(CC)CC)OCC(CC)CC
SWQWONXMUXCEDF-UHFFFAOYSA-N
0.000
abstract
1

MQHSFMJHURNQIE-UHFFFAOYSA-N
tetrakis(2-ethylhexyl) silicate
Chemical compound

CCCCC(CC)CO[Si](OCC(CC)CCCC)(OCC(CC)CCCC)OCC(CC)CCCC
MQHSFMJHURNQIE-UHFFFAOYSA-N
0.000
abstract
1

229960002622
triacetin
Drugs

0.000
abstract
1

MWOOGOJBHIARFG-UHFFFAOYSA-N
vanillin
Chemical compound

COC1=CC(C=O)=CC=C1O
MWOOGOJBHIARFG-UHFFFAOYSA-N
0.000
abstract
1

FGQOOHJZONJGDT-UHFFFAOYSA-N
vanillin
Natural products

COC1=CC(O)=CC(C=O)=C1
FGQOOHJZONJGDT-UHFFFAOYSA-N
0.000
abstract
1

235000012141
vanillin
Nutrition

0.000
abstract
1

229920002554
vinyl polymer
Polymers

0.000
abstract
1

238000004073
vulcanization
Methods

0.000
abstract
1

239000002759
woven fabric
Substances

0.000
abstract
1

YISPIDBWTUCKKH-UHFFFAOYSA-L
zinc;4-methylbenzenesulfonate
Chemical compound

[Zn+2].CC1=CC=C(S([O-])(=O)=O)C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1
YISPIDBWTUCKKH-UHFFFAOYSA-L
0.000
abstract
1

ZMCVIGZGZXZJKM-UHFFFAOYSA-L
zinc;benzenesulfonate
Chemical compound

[Zn+2].[O-]S(=O)(=O)C1=CC=CC=C1.[O-]S(=O)(=O)C1=CC=CC=C1
ZMCVIGZGZXZJKM-UHFFFAOYSA-L
0.000
abstract
1

239000004711
α-olefin
Substances

0.000
abstract
1

Classifications

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients

C08K5/00—Use of organic ingredients

C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds

C08K5/41—Compounds containing sulfur bound to oxygen

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients

C08K5/00—Use of organic ingredients

C08K5/0008—Organic ingredients according to more than one of the «one dot» groups of C08K5/01 – C08K5/59

C08K5/005—Stabilisers against oxidation, heat, light, ozone

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients

C08K5/00—Use of organic ingredients

C08K5/04—Oxygen-containing compounds

C08K5/07—Aldehydes; Ketones

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients

C08K5/00—Use of organic ingredients

C08K5/04—Oxygen-containing compounds

C08K5/10—Esters; Ether-esters

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients

C08K5/00—Use of organic ingredients

C08K5/54—Silicon-containing compounds

C08K5/541—Silicon-containing compounds containing oxygen

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS

C08L21/00—Compositions of unspecified rubbers

Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10S428/00—Stock material or miscellaneous articles

Y10S428/92—Fire or heat protection feature

Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10S524/00—Synthetic resins or natural rubbers — part of the class 520 series

Y10S524/925—Natural rubber compositions having nonreactive materials, i.e. NRM, other than: carbon, silicon dioxide, glass titanium dioxide, water, hydrocarbon or halohydrocarbon

Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T156/00—Adhesive bonding and miscellaneous chemical manufacture

Y10T156/10—Methods of surface bonding and/or assembly therefor

Y10T156/1089—Methods of surface bonding and/or assembly therefor of discrete laminae to single face of additional lamina

Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/31504—Composite [nonstructural laminate]

Y10T428/31786—Of polyester [e.g., alkyd, etc.]

Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]

Y10T442/30—Woven fabric [i.e., woven strand or strip material]

Y10T442/3854—Woven fabric with a preformed polymeric film or sheet

Y10T442/3911—Natural or synthetic rubber sheet or film

Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]

Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]

Y10T442/674—Nonwoven fabric with a preformed polymeric film or sheet

Y10T442/679—Natural or synthetic rubber sheet or film

Abstract

1304927 Rubber and polyester fibre laminates UNIROYAL Inc 13 March 1970 [17 March 1969] 12096/70 Heading B5N [Also in Division C3] The adhesion of rubber compositions containing amines or amine-yielding substances, e.g. accelerators, to polyester textiles isimproved by adding a deterioration preventing substance effective to interact with the amine or amine yielding substance to mitigate its effect to the composition before the application and vulcanization of the rubber on the textile. The deterioration preventing substance is selected from benzaldehyde, salicylaldehyde, 3-chloromethyl salicylaldehyde, 3-chloromethyl-5- hydroxybenzaldehyde, furfural, m-hydroxy. benzaldehyde, p-hydroxybenzaldehyde, 2,4- dihydroxybenzaldehyde, 2,4-dimethoxy benzaldehyde, 2,3-dimethoxy benzaldehyde, vanillin, verataldehyde, 5-methoxy salicylaldehyde, cinnamic aldehyde, 2 – ethyl – 4 – hexanal, p – isopropyl benzaldehyde, 2,2 – dimethyl – 3,4- octadienal, terephthaldehyde, dialkyl oxalates, butyl butyrate, butyl lactate, ethyl carbonate, ethyl succinate, dimethyl terephthalate, 2- ethylhexyl acrylate, ethyl p-toluene sulphonate, triacetin, methyl salicylate, butyrolactone, 2,2,4-trimethyl pentenolactone, linear or cyclic lactide polymers, tetramethyl-1,3-butanedione, benzil, benzoin, 1,3 – cyclohexanedione, pquinone, dimedone, 1,3 – dihydroxypropanenone, d,l-camphor, dehydroacetic acid, 2,5- dicarbethoxy-1,4-cyclohexandione, acetoacetic esters, butyl pyruvate, triglycol dichloride, benzyl chloride, p-xylene dichloride, α,α,α-trichlorotoluene, 1,4 – bis – (trichloromethyl) benzene, aniline hydrochloride, dianiline-1,5- naphthalenedisulphonate, zinc – p – toluenesulphonate, zinc benzenesulphonate, sodium 2- formyl benzenesulphonate, tetraethyl orthosilicate, tetra – (2 – ethyl – hexyl) orthosilicate, tetra – (2 – ethyl butyl) orthosilicate, triisodecyl orthoformate, vinyl triethoxy-silane, 2 – nitro – 2 – methyl – 1, 3 – propanediol sulphite, m-phenylene diisocyanate, phenyl-isothiocyanate, vinyl cyclohexene dioxide, styrene oxide; epichlorohydrin-bisphenol A condensate epoxy resins, isotoric anhydride, dodecenyl sucoinic anhydride, octadecenyl succinic anhydride, polyglyoxal, polyvinyl acetate, trialdehyde starch or poly-(methylvinyl ketone). The rubber composition may comprise natural or synthetic rubbers such as polybutadiene; polyisoprene, polychloroprene, copolymers of dienes with styrene, acrylonitrile, vinyl pyridene, ethyl acrylate, isobutylene or copolymers of at least 2 α-olefins such as ethylene, propylene or butene-1 with one or more polyenes, especially the non-conjugated dienes such as dicyelopentadiene, ethylidene norbornene, methylene norbornene, cyclo-octadiene, tetra-hydroindene of 1,4-hexadiene. The composition may also contain vulcanizing agents, activators, tackifiers, lubricants, retarders, antioxidants, antiozonants, peptizers, extenders, fillers and pigments. The polyester textile may be in the form of mono- or multifilaments, plied yarns, cords, staple fibres, woven fabrics or non-woven mats. Adhesives, e.g. rubber latices may be applied to fabric by spraying, dipping, painting or spreading before application of the rubber compositions. The rubber-textile composites are suitable for use in the construction of tyres.

GB1209670A
1969-03-17
1970-03-13

Expired

GB1304927A
(en)

Applications Claiming Priority (1)

Application Number
Priority Date
Filing Date
Title

US80791169A

1969-03-17
1969-03-17

Publications (1)

Publication Number
Publication Date

GB1304927A
true

GB1304927A
(en)

1973-01-31

Family
ID=25197409
Family Applications (1)

Application Number
Title
Priority Date
Filing Date

GB1209670A
Expired

GB1304927A
(en)

1969-03-17
1970-03-13

Country Status (9)

Country
Link

US
(1)

US3658637A
(en)

AT
(1)

AT316134B
(en)

BE
(1)

BE747411A
(en)

BR
(1)

BR7017517D0
(en)

DE
(1)

DE2012416A1
(en)

FR
(3)

FR2037211B1
(en)

GB
(1)

GB1304927A
(en)

LU
(1)

LU60534A1
(en)

NL
(1)

NL7003677A
(en)

Cited By (1)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US20170292012A1
(en)

*

2016-04-07
2017-10-12
The Goodyear Tire & Rubber Company
Rubber comprised of product of diene-based elastomer, branched polyethylenimine oligomer and reinforcing filler, and tire with component

Families Citing this family (16)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US4009304A
(en)

*

1971-09-30
1977-02-22
Air Products And Chemicals, Inc.
Fluorinated polyester tire reinforcement materials

US3793132A
(en)

*

1972-02-23
1974-02-19
Goodyear Tire & Rubber
Modified polyester and rubber structures made therefrom

US3883460A
(en)

*

1973-04-16
1975-05-13
Firestone Tire & Rubber Co
Stabilization of polybutadiene resin

US3890260A
(en)

*

1973-04-16
1975-06-17
Firestone Tire & Rubber Co
Stabilized polybutadiene resins

US3883457A
(en)

*

1973-04-16
1975-05-13
Firestone Tire & Rubber Co
Stabilized polybutadiene resin

US3886106A
(en)

*

1973-04-16
1975-05-27
Firestone Tire & Rubber Co
Stabilization of polybutadiene resin

US4073776A
(en)

*

1975-01-28
1978-02-14
Schenectady Chemicals, Inc.
Tackifiers for elastomers

AU3658378A
(en)

*

1977-07-11
1979-12-06
American Cyanamid Co
Rubber accelerators

US4228045A
(en)

*

1979-01-31
1980-10-14
American Cyanamid Company
Method of adhesion of rubber to reinforcing materials

US6121211A
(en)

*

1998-07-17
2000-09-19
The Lubrizol Corporation
Engine oil having dithiocarbamate and aldehyde/epoxide for improved seal performance, sludge and deposit performance

CA2277412A1
(en)

*

1998-07-17
2000-01-17
The Lubrizol Corporation
Engine oil having dispersant and aldehyde/epoxide for improved seal performance, sludge and deposit performance

EP2675839B1
(en)

*

2011-02-17
2019-08-14
Milliken & Company
Adhesion composition and textile materials and articles treated therewith

US20120214372A1
(en)

2011-02-17
2012-08-23
Shulong Li
Adhesion Composition and Textile Materials and Articles Treated Therewith

JP2017115106A
(en)

*

2015-12-25
2017-06-29
株式会社クレハ
Composition, composition for down hole tool, degradable rubber member for down hole, down hole tool and winze excavation method

CA3057580C
(en)

2017-05-25
2020-05-26
Kureha Corporation
Rubber composition for downhole tools and member for downhole tools

CN112745470B
(en)

*

2021-01-14
2022-05-06
江苏海洋大学
Application of unsaturated pyridinium inner salt in preparation of blocked polyurethane prepolymer

Family Cites Families (6)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

GB531286A
(en)

*

1939-07-17
1941-01-01
Thomas Lorimer
Improvements in and relating to dabbing brushes for woolcombing machines

US3411980A
(en)

*

1965-03-26
1968-11-19
Goodyear Tire & Rubber
In-situ resin adhesion of reinforcing element-to-rubber

US3419463A
(en)

*

1965-11-12
1968-12-31
Celanese Corp
Adhesion of polyester to rubber

US3487056A
(en)

*

1967-03-13
1969-12-30
Pennwalt Corp
Bis(dialkylammonium)oxalates as accelerator activators in the vulcanization of elastomers

US3411970A
(en)

*

1967-11-01
1968-11-19
Gen Tire & Rubber Co
Formation of laminates of rubber and cord

US3506624A
(en)

*

1968-03-11
1970-04-14
Rudolf Adolf Behrens
Elastomer compositions vulcanized with sulfur,a salt of an organic acid,and a maleimide compound

1969

1969-03-17
US
US3658637D
patent/US3658637A/en
not_active
Expired – Lifetime

1970

1970-03-13
GB
GB1209670A
patent/GB1304927A/en
not_active
Expired

1970-03-16
BE
BE747411D
patent/BE747411A/en
unknown

1970-03-16
NL
NL7003677A
patent/NL7003677A/xx
unknown

1970-03-16
DE
DE19702012416
patent/DE2012416A1/en
active
Pending

1970-03-16
FR
FR7009343A
patent/FR2037211B1/fr
not_active
Expired

1970-03-17
LU
LU60534D
patent/LU60534A1/xx
unknown

1970-03-17
BR
BR21751770A
patent/BR7017517D0/en
unknown

1970-03-17
AT
AT248870A
patent/AT316134B/en
not_active
IP Right Cessation

1973

1973-07-17
FR
FR7326142A
patent/FR2187544A1/fr
not_active
Withdrawn

1973-07-17
FR
FR7326143A
patent/FR2187545A1/fr
not_active
Withdrawn

Cited By (2)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US20170292012A1
(en)

*

2016-04-07
2017-10-12
The Goodyear Tire & Rubber Company
Rubber comprised of product of diene-based elastomer, branched polyethylenimine oligomer and reinforcing filler, and tire with component

US10005896B2
(en)

*

2016-04-07
2018-06-26
The Goodyear Tire & Rubber Company
Rubber comprised of product of diene-based elastomer, branched polyethylenimine oligomer and reinforcing filler, and tire with component

Also Published As

Publication number
Publication date

US3658637A
(en)

1972-04-25

AT316134B
(en)

1974-06-25

BR7017517D0
(en)

1973-02-20

FR2187544A1
(en)

1974-01-18

DE2012416A1
(en)

1970-09-24

FR2037211B1
(en)

1975-07-04

LU60534A1
(en)

1970-05-21

BE747411A
(en)

1970-09-16

FR2187545A1
(en)

1974-01-18

NL7003677A
(en)

1970-09-21

FR2037211A1
(en)

1970-12-31

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Legal Events

Date
Code
Title
Description

1973-06-13
PS
Patent sealed [section 19, patents act 1949]

1975-10-08
PLNP
Patent lapsed through nonpayment of renewal fees

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