CA1103280A - Alkali resistant, mineral fibres - Google Patents
Alkali resistant, mineral fibresInfo
- Publication number
- CA1103280A CA1103280A CA318,934A CA318934A CA1103280A CA 1103280 A CA1103280 A CA 1103280A CA 318934 A CA318934 A CA 318934A CA 1103280 A CA1103280 A CA 1103280A
- Authority
- CA
- Canada
- Prior art keywords
- fibres
- mineral fibres
- alkali resistant
- alkali
- synthetic
- Prior art date
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C13/00—Fibre or filament compositions
- C03C13/001—Alkali-resistant fibres
- C03C13/002—Alkali-resistant fibres containing zirconium
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C13/00—Fibre or filament compositions
- C03C13/001—Alkali-resistant fibres
Abstract
Abstract of the Disclosure.
Alkali resistant, synthetic, mineral fibres having the following composition on weight basis: SiO2: 42-50%, Al2O3: 8-13%, Iron Oxides (calculated as FeO): 6-11%, CaO: 4-11%, MgO: 17-22%, TiO2: 0.5-3% and alkali metal oxides: 0.5-3.5%.
Alkali resistant, synthetic, mineral fibres having the following composition on weight basis: SiO2: 42-50%, Al2O3: 8-13%, Iron Oxides (calculated as FeO): 6-11%, CaO: 4-11%, MgO: 17-22%, TiO2: 0.5-3% and alkali metal oxides: 0.5-3.5%.
Description
This invention relates to alkali resistan-t, synthetic, mineral fibres and ~ore particularly mineral fibres for the reinforcement of cementitious products.
Cementitious products, such as products made of con-crete, based on Portland cement or other types of cementor mixtures of cement and other types of binders, exhibit high compression strengths but low -tensile strengths.
It is well known that the tensile strengths of cemen-titious products can be increased by incorporating there-10 in a fibrous reinforcement. Thus, asbestos fibres havefound widespread use as a reinforcing material in cement products for use in the building industry.
Unfortunately, the use of asbestos fibres presents serious health problems and, therefore, the use of as-15 bestos fibres has been prohibited in some countries andis likely to be prohibited in other countries.
Many attempts have been made to replace asbestos fibres with synthetic mineral fibres, such as rock wool fibres, slag fibres and glass fibres in fibre reinforced 20 cementitious products.
However, cementitious products reinforced by synthe-tic mineral fibres do not exhibit fully satisfactory strength properties because the mineral fibres do not have a sufficient resistance to attack by the alkaline 25 components of the cement matrix to prevent the fibres from being partially or wholly decomposed.
According to the accepted German patent application No. 1.796.213 it has been attempted to increase the alka-li resistance of glass fibres by coating the fibres with 30 a methyl siloxane and by manufacturing the glass fibres from such starting materials that the fibres produced have a composition falling within the following ranges:
SiO2: 35-47% by weight A:L2O3: 5-13% _ _ FeO+Fe2o3:2-15~ - -C~IO: 2-23%
MgO: 1-30%
Na2O~K2O:up to 4%
T:iO2: up to 10% - - and either ZrO2: up to 10% - - or Z}lO: up to 5%
Cementitious products, such as products made of con-crete, based on Portland cement or other types of cementor mixtures of cement and other types of binders, exhibit high compression strengths but low -tensile strengths.
It is well known that the tensile strengths of cemen-titious products can be increased by incorporating there-10 in a fibrous reinforcement. Thus, asbestos fibres havefound widespread use as a reinforcing material in cement products for use in the building industry.
Unfortunately, the use of asbestos fibres presents serious health problems and, therefore, the use of as-15 bestos fibres has been prohibited in some countries andis likely to be prohibited in other countries.
Many attempts have been made to replace asbestos fibres with synthetic mineral fibres, such as rock wool fibres, slag fibres and glass fibres in fibre reinforced 20 cementitious products.
However, cementitious products reinforced by synthe-tic mineral fibres do not exhibit fully satisfactory strength properties because the mineral fibres do not have a sufficient resistance to attack by the alkaline 25 components of the cement matrix to prevent the fibres from being partially or wholly decomposed.
According to the accepted German patent application No. 1.796.213 it has been attempted to increase the alka-li resistance of glass fibres by coating the fibres with 30 a methyl siloxane and by manufacturing the glass fibres from such starting materials that the fibres produced have a composition falling within the following ranges:
SiO2: 35-47% by weight A:L2O3: 5-13% _ _ FeO+Fe2o3:2-15~ - -C~IO: 2-23%
MgO: 1-30%
Na2O~K2O:up to 4%
T:iO2: up to 10% - - and either ZrO2: up to 10% - - or Z}lO: up to 5%
- 2 -the sum of CaO and MgO being from 14 to 38~ by weigh-t.
The invention is based on detailed inves-tiga-tions on the influence oE various oxides on the tensile strength and alkali resistance of -the fibres made from mixtures of such oxides. During these investigations it was found -that apart from the tensile s-treng-t:h and alkali resis-tance of of fibres a further factor, viz. -the melt viscosi-ty, has to be taken into consideration in order to provide fibres suitable for commercial production. It was also ~ound that 10 mixtures having high contents of alkaline components did not form melts having a viscosity suitable for fibre pro-aUCtion.
Based on comprehensive investigations and computercalculations it was found that synthetic mineral fibres 15 having high tensile strength and alkali resistance can be produced from melts having a satisfactory viscosity.
Thus, the fibres according to the invention have the following composition:
20 SiO2: 42-50% by weight 2 3 8-13%
Iron oxides (calculated as FeO) 6-11% - -CaO: 4-11%
25 MgO: 17-22%
TiO2: 0-5-3%
R2O 0.5-3 5%
wherein R is an alkali metal.
Melts having a composition corresponding to the 30 fibre composition set forth above have a viscosity of about 5 poise at about 1500C. This is a fully satis-factory viscosity since it is well known that the melt viscosity should be from about 5 to about 10 poise at 1500C to be suitable for fibre production.
The al}cali resistance of the fibres according to the invention was determined by using the accelerated alkali resistance test described by Majumdar, A.J., and Ryder, J.F." "Glass Fibre Reinforcement of Cement Pro-~-~ii 3~
ducts", Glass Technology, Volume 8, No. 3 (June 1968).
The strength and alkali resistanee of fibres accord-ing to the invention will appear from -the table set forth in the Example.
The invention also rela-tes to cementitious products reinforced by the alkali resis-tant synthetic mineral fibres described above.
When the synthetic mineral fibres according -to the invention are to be used for the reinforcement of cemen-10 titious products, such as products based on Portland cement, calcium silicate or similar alkaline binders, the average diameter of the fibres preferably is from
The invention is based on detailed inves-tiga-tions on the influence oE various oxides on the tensile strength and alkali resistance of -the fibres made from mixtures of such oxides. During these investigations it was found -that apart from the tensile s-treng-t:h and alkali resis-tance of of fibres a further factor, viz. -the melt viscosi-ty, has to be taken into consideration in order to provide fibres suitable for commercial production. It was also ~ound that 10 mixtures having high contents of alkaline components did not form melts having a viscosity suitable for fibre pro-aUCtion.
Based on comprehensive investigations and computercalculations it was found that synthetic mineral fibres 15 having high tensile strength and alkali resistance can be produced from melts having a satisfactory viscosity.
Thus, the fibres according to the invention have the following composition:
20 SiO2: 42-50% by weight 2 3 8-13%
Iron oxides (calculated as FeO) 6-11% - -CaO: 4-11%
25 MgO: 17-22%
TiO2: 0-5-3%
R2O 0.5-3 5%
wherein R is an alkali metal.
Melts having a composition corresponding to the 30 fibre composition set forth above have a viscosity of about 5 poise at about 1500C. This is a fully satis-factory viscosity since it is well known that the melt viscosity should be from about 5 to about 10 poise at 1500C to be suitable for fibre production.
The al}cali resistance of the fibres according to the invention was determined by using the accelerated alkali resistance test described by Majumdar, A.J., and Ryder, J.F." "Glass Fibre Reinforcement of Cement Pro-~-~ii 3~
ducts", Glass Technology, Volume 8, No. 3 (June 1968).
The strength and alkali resistanee of fibres accord-ing to the invention will appear from -the table set forth in the Example.
The invention also rela-tes to cementitious products reinforced by the alkali resis-tant synthetic mineral fibres described above.
When the synthetic mineral fibres according -to the invention are to be used for the reinforcement of cemen-10 titious products, such as products based on Portland cement, calcium silicate or similar alkaline binders, the average diameter of the fibres preferably is from
3 to 15 ~m. If the average diameter is less tha'n 3 ~m, the reduction of strength produced by the alkaline compo-15 nents of the matrix is excessively high. On the other hand, fibres having an average diameter exceeding 15 ~m should preferably not be used because the reinforcement per area unit of a cross section of a fibre reinforced product decreases with increasing fibre diameter.
The invention will be described in further detail with reference to the following Example illustrating the manufacture of synthetic mineral fibres of different compositions.
Synthetic mineral fibres were produced from the fol-lowing starting materials: diabase, lime, magnesite, corundum, titanium dioxide and quartz. The mixture of starting materials were molten in a crucible and the melt 30 was converted into fibres with a cascade spinner.
The composition of the fibres thus produced and their properties are set forth in the following Table:
~L~$3J~I~V
o o ~ U~ U~Lr) o U~ ~ o ~D , , , . . . . r~ ~r~
tn ~ ~ ~D CO cn ~ ~ n ~r ~
u~ o o o ~ h Lt) . , , , . , . oo o~ ~ ~ Q~
u~cc~ D ~ O ~ ~ In ~ u t~l aJ ~ U~
~D ~ ~
U~ U~ LOLr) O O O 00 ~D ~ U~ rd ~ra~
~9 ~ a o In o o ~ In o a~ ~r ' . . . . . . . ~ ~, . U~
i~ ~~ O ~ ~ ~_ -rl er ~ ~ ~ rQ
0 In o u~ Ln O O ~9 0 u~ ~ ~ ~ ~ o ~ ~ r- ~-~r o In o n LO u~ o ~D In ~ ~ X r1 U~
. . . . . . . ~ ' O '~
~nc~ 5~
~r ~ ~ P~ ~ O
U~ U~ In O U~ O O ~ ~ ~ ~ a) u, ~ ~ ~ o ~r . O ~ O
m x ~r N a~ ~ ~0 ~ O ~
¢ Il') O 11~ 0 0Il~ O O~ ~ ~ X a) ~,X
~ . , . . . . . ~ ~ . t~
U~t` N ~ 00 I_ ~ ~ ~ ~ O t) ;c u~ o In n o o L~ o ~ ~ 3 ~ k u~ ~ o ~_ ~ ~ ~ ~ , ~ o a) a) ~
O
~9 X o o o o n o ou~ ~ I` o . . . . . . . ~ , ~ ~ U7 ~ ~o a) o O R
o u~ o Ln oLrl o o Ln r~
. . . . . . . O ~
O ~ ~ o~ ~ o ~ ~7 ~ ~ O Q) P;~r ~ ~ ~ .,~
3~ ;~
r~
u~
~ Q ~
~ ~ rd o o ,- .
0\
3 ~ 0 U~ , N ~ ~ N
O ~ ~ Q = = = U~ a)a~
,~
~ ~r~ op : r~
. o\O = O O~ ~ ~ rl $ ~ ~
o ~ ~ aJ ` a) ~
Cl~ N O ~ h ~ ~ N ~ Q O(11 r~ ~ ~1 E~i O ~ O O O O O O S-l X u~
O ~ rd ~ rl N ~1 ~ ,_1 ot.) O
C) U~ P I UJ~ h ~¢ --As will appear from the above data the fibres accord-ing to the invention which have essentially the same strength as -the well known rock wool fibres exhibit a con-siderably higher alkali resistance. Further, it should be noted that -the acidity which reflects the viscosity of the mel-t from which the fibres are prepared and which prefer-ably should be within -the ranc3e 1.05-1.50 is fully accept-able.
The invention will be described in further detail with reference to the following Example illustrating the manufacture of synthetic mineral fibres of different compositions.
Synthetic mineral fibres were produced from the fol-lowing starting materials: diabase, lime, magnesite, corundum, titanium dioxide and quartz. The mixture of starting materials were molten in a crucible and the melt 30 was converted into fibres with a cascade spinner.
The composition of the fibres thus produced and their properties are set forth in the following Table:
~L~$3J~I~V
o o ~ U~ U~Lr) o U~ ~ o ~D , , , . . . . r~ ~r~
tn ~ ~ ~D CO cn ~ ~ n ~r ~
u~ o o o ~ h Lt) . , , , . , . oo o~ ~ ~ Q~
u~cc~ D ~ O ~ ~ In ~ u t~l aJ ~ U~
~D ~ ~
U~ U~ LOLr) O O O 00 ~D ~ U~ rd ~ra~
~9 ~ a o In o o ~ In o a~ ~r ' . . . . . . . ~ ~, . U~
i~ ~~ O ~ ~ ~_ -rl er ~ ~ ~ rQ
0 In o u~ Ln O O ~9 0 u~ ~ ~ ~ ~ o ~ ~ r- ~-~r o In o n LO u~ o ~D In ~ ~ X r1 U~
. . . . . . . ~ ' O '~
~nc~ 5~
~r ~ ~ P~ ~ O
U~ U~ In O U~ O O ~ ~ ~ ~ a) u, ~ ~ ~ o ~r . O ~ O
m x ~r N a~ ~ ~0 ~ O ~
¢ Il') O 11~ 0 0Il~ O O~ ~ ~ X a) ~,X
~ . , . . . . . ~ ~ . t~
U~t` N ~ 00 I_ ~ ~ ~ ~ O t) ;c u~ o In n o o L~ o ~ ~ 3 ~ k u~ ~ o ~_ ~ ~ ~ ~ , ~ o a) a) ~
O
~9 X o o o o n o ou~ ~ I` o . . . . . . . ~ , ~ ~ U7 ~ ~o a) o O R
o u~ o Ln oLrl o o Ln r~
. . . . . . . O ~
O ~ ~ o~ ~ o ~ ~7 ~ ~ O Q) P;~r ~ ~ ~ .,~
3~ ;~
r~
u~
~ Q ~
~ ~ rd o o ,- .
0\
3 ~ 0 U~ , N ~ ~ N
O ~ ~ Q = = = U~ a)a~
,~
~ ~r~ op : r~
. o\O = O O~ ~ ~ rl $ ~ ~
o ~ ~ aJ ` a) ~
Cl~ N O ~ h ~ ~ N ~ Q O(11 r~ ~ ~1 E~i O ~ O O O O O O S-l X u~
O ~ rd ~ rl N ~1 ~ ,_1 ot.) O
C) U~ P I UJ~ h ~¢ --As will appear from the above data the fibres accord-ing to the invention which have essentially the same strength as -the well known rock wool fibres exhibit a con-siderably higher alkali resistance. Further, it should be noted that -the acidity which reflects the viscosity of the mel-t from which the fibres are prepared and which prefer-ably should be within -the ranc3e 1.05-1.50 is fully accept-able.
Claims (4)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:-CLAIMS:
1. Alkali resistant, synthetic, mineral fibres, c h a r a c t e r i z e d in that they have -the follow-ing composition:
SiO2: 42-50% by weight Al2O3: 8-13% - -Iron oxides (calculated as FeO): 6-11% - -CaO: 4-11% - -MgO: 17-22% - -TiO2: 0.5-3% - -R2O: 0.5-3.5% - -wherein R is an alkali metal.
SiO2: 42-50% by weight Al2O3: 8-13% - -Iron oxides (calculated as FeO): 6-11% - -CaO: 4-11% - -MgO: 17-22% - -TiO2: 0.5-3% - -R2O: 0.5-3.5% - -wherein R is an alkali metal.
2. A fibre reinforced cementitious product, c h a r a c t e r i z e d in that the fibre reinforce-ment comprises alkali resistant, synthetic, mineral fibres having the following composition:
SiO2: 42-50% by weight Al2O3: 8-13% - -Iron oxides (calculated as FeO): 6-11% - -CaO: 4-11% - -MgO: 17-22% - -TiO2: 0.5-3% - -R2O: 0.5-3,5% - -wherein R is an alkali metal.
SiO2: 42-50% by weight Al2O3: 8-13% - -Iron oxides (calculated as FeO): 6-11% - -CaO: 4-11% - -MgO: 17-22% - -TiO2: 0.5-3% - -R2O: 0.5-3,5% - -wherein R is an alkali metal.
3. A fibre reinforced cementitious product as in claim 2, c h a r a c t e r i z e d in that the mineral fibres have an average diameter of between 3 and 15 µm.
4. A fibre reinforced cementitious product as in claim 2, c h a r a c t e r i z e d in that the cementi-tious matrix consists of Portland cement.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DK1078A DK143938C (en) | 1978-01-02 | 1978-01-02 | ALKALIR RESISTANT, SYNTHETIC MINERAL FIBERS AND FIBER REINFORCED PRODUCTS BASED ON CEMENT OR CALCIUM SILICATE AS A BINDING AGENT |
DK10/78 | 1978-01-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1103280A true CA1103280A (en) | 1981-06-16 |
Family
ID=8088719
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA318,934A Expired CA1103280A (en) | 1978-01-02 | 1979-01-02 | Alkali resistant, mineral fibres |
Country Status (19)
Country | Link |
---|---|
US (1) | US4205992A (en) |
JP (1) | JPS54101922A (en) |
AT (1) | AT394709B (en) |
AU (1) | AU517965B2 (en) |
BE (1) | BE873263A (en) |
CA (1) | CA1103280A (en) |
CH (1) | CH637907A5 (en) |
DE (1) | DE2856206A1 (en) |
DK (1) | DK143938C (en) |
ES (1) | ES476530A1 (en) |
FI (1) | FI63559C (en) |
FR (1) | FR2413335A1 (en) |
GB (1) | GB2011379B (en) |
IE (1) | IE47772B1 (en) |
IT (1) | IT1109909B (en) |
NL (1) | NL185716C (en) |
NO (1) | NO144205C (en) |
PT (1) | PT68984A (en) |
SE (1) | SE432417C (en) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS605539B2 (en) * | 1980-03-17 | 1985-02-12 | 日東紡績株式会社 | Alkali-resistant, heat-resistant inorganic fiber |
US4560606A (en) * | 1981-11-16 | 1985-12-24 | Owens-Corning Fiberglas Corporation | Basalt compositions and their fibers |
JPS58502054A (en) * | 1981-12-04 | 1983-12-01 | アメリカ合衆国 | Resistant to alkali glass fiber |
WO1993015028A1 (en) * | 1992-01-17 | 1993-08-05 | The Morgan Crucible Company Plc | Saline soluble inorganic fibres |
US5994247A (en) * | 1992-01-17 | 1999-11-30 | The Morgan Crucible Company Plc | Saline soluble inorganic fibres |
DK156692D0 (en) * | 1992-12-29 | 1992-12-29 | Rockwool Int | MINERAL FIBER PRODUCT |
ES2196040T3 (en) * | 1993-01-15 | 2003-12-16 | Morgan Crucible Co | INORGANIC FIBERS SOLUBLE IN SALIN DISSOLUTIONS. |
US5811360A (en) * | 1993-01-15 | 1998-09-22 | The Morgan Crucible Company Plc | Saline soluble inorganic fibres |
PL177839B1 (en) * | 1994-02-11 | 2000-01-31 | Rockwool Int | Man-made glass fibres |
FR2717464B1 (en) * | 1994-03-15 | 1996-05-24 | Vetrotex France Sa | Glass fibers intended for the reinforcement of organic and composite materials obtained. |
US5691255A (en) * | 1994-04-19 | 1997-11-25 | Rockwool International | Man-made vitreous fiber wool |
GB9508683D0 (en) * | 1994-08-02 | 1995-06-14 | Morgan Crucible Co | Inorganic fibres |
EP0792843A3 (en) * | 1994-11-08 | 1998-08-19 | Rockwool International A/S | Man-made vitreous fibres |
US5928975A (en) * | 1995-09-21 | 1999-07-27 | The Morgan Crucible Company,Plc | Saline soluble inorganic fibers |
US6346494B1 (en) | 1995-11-08 | 2002-02-12 | Rockwool International A/S | Man-made vitreous fibres |
US6077798A (en) * | 1996-08-02 | 2000-06-20 | Owens Corning Fiberglas Technology, Inc. | Biosoluble, high temperature mineral wools |
GB2341607B (en) | 1998-09-15 | 2000-07-19 | Morgan Crucible Co | Bonded fibrous materials |
WO2001019744A1 (en) | 1999-09-10 | 2001-03-22 | The Morgan Crucible Company Plc | High temperature resistant saline soluble fibres |
DE10010664B4 (en) * | 2000-03-04 | 2007-05-24 | Asglawo Technofibre Gmbh | Reinforcing fibers for cement-bonded concrete elements |
CA2402886C (en) | 2000-03-14 | 2012-02-14 | James Hardie Research Pty Limited | Fiber cement building materials with low density additives |
GB2383793B (en) * | 2002-01-04 | 2003-11-19 | Morgan Crucible Co | Saline soluble inorganic fibres |
MXPA05002057A (en) * | 2002-08-23 | 2005-09-12 | James Hardie Int Finance Bv | Synthetic hollow microspheres. |
US7993570B2 (en) | 2002-10-07 | 2011-08-09 | James Hardie Technology Limited | Durable medium-density fibre cement composite |
US20090146108A1 (en) * | 2003-08-25 | 2009-06-11 | Amlan Datta | Methods and Formulations for Producing Low Density Products |
US20090156385A1 (en) * | 2003-10-29 | 2009-06-18 | Giang Biscan | Manufacture and use of engineered carbide and nitride composites |
US7998571B2 (en) | 2004-07-09 | 2011-08-16 | James Hardie Technology Limited | Composite cement article incorporating a powder coating and methods of making same |
US7875566B2 (en) * | 2004-11-01 | 2011-01-25 | The Morgan Crucible Company Plc | Modification of alkaline earth silicate fibres |
EP1856003A2 (en) * | 2005-02-24 | 2007-11-21 | James Hardie International Finance B.V. | Alkali resistant glass compositions |
CA2632760C (en) * | 2005-12-08 | 2017-11-28 | James Hardie International Finance B.V. | Engineered low-density heterogeneous microparticles and methods and formulations for producing the microparticles |
US8993462B2 (en) | 2006-04-12 | 2015-03-31 | James Hardie Technology Limited | Surface sealed reinforced building element |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3901720A (en) * | 1966-07-11 | 1975-08-26 | Nat Res Dev | Glass fibres and compositions containing glass fibres |
DE1796213B2 (en) * | 1967-09-26 | 1976-01-02 | Ceskoslovenska Akademie Ved., Prag | Fiber reinforced cement |
US3736162A (en) * | 1972-02-10 | 1973-05-29 | Ceskoslovenska Akademie Ved | Cements containing mineral fibers of high corrosion resistance |
JPS5611667B2 (en) * | 1972-06-09 | 1981-03-16 | ||
US3929497A (en) * | 1973-01-31 | 1975-12-30 | Fiberglas Canada Ltd | Crystallizable glass suitable for fiber production |
JPS5342332B2 (en) * | 1975-01-30 | 1978-11-10 | ||
US4002482A (en) * | 1975-02-14 | 1977-01-11 | Jenaer Glaswerk Schott & Gen. | Glass compositions suitable for incorporation into concrete |
US4008094A (en) * | 1975-07-16 | 1977-02-15 | Corning Glass Works | High durability, reinforcing fibers for cementitious materials |
-
1978
- 1978-01-02 DK DK1078A patent/DK143938C/en not_active IP Right Cessation
- 1978-12-27 PT PT68984A patent/PT68984A/en unknown
- 1978-12-27 DE DE19782856206 patent/DE2856206A1/en active Granted
- 1978-12-28 JP JP16444678A patent/JPS54101922A/en active Granted
- 1978-12-28 US US05/974,005 patent/US4205992A/en not_active Expired - Lifetime
- 1978-12-29 SE SE7813427A patent/SE432417C/en not_active IP Right Cessation
- 1978-12-29 FI FI784052A patent/FI63559C/en not_active IP Right Cessation
- 1978-12-29 FR FR7836888A patent/FR2413335A1/en active Granted
- 1978-12-29 AT AT0936978A patent/AT394709B/en not_active IP Right Cessation
- 1978-12-29 GB GB7850294A patent/GB2011379B/en not_active Expired
- 1978-12-29 NO NO78784417A patent/NO144205C/en unknown
- 1978-12-29 CH CH1326978A patent/CH637907A5/en not_active IP Right Cessation
-
1979
- 1979-01-02 ES ES476530A patent/ES476530A1/en not_active Expired
- 1979-01-02 IE IE8/79A patent/IE47772B1/en not_active IP Right Cessation
- 1979-01-02 CA CA318,934A patent/CA1103280A/en not_active Expired
- 1979-01-02 BE BE192722A patent/BE873263A/en not_active IP Right Cessation
- 1979-01-02 AU AU43056/79A patent/AU517965B2/en not_active Ceased
- 1979-01-02 IT IT19016/79A patent/IT1109909B/en active
- 1979-01-02 NL NLAANVRAGE7900010,A patent/NL185716C/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
AU517965B2 (en) | 1981-09-03 |
GB2011379A (en) | 1979-07-11 |
FR2413335A1 (en) | 1979-07-27 |
US4205992A (en) | 1980-06-03 |
IE790008L (en) | 1979-07-02 |
SE7813427L (en) | 1979-07-03 |
DE2856206A1 (en) | 1979-07-12 |
FI63559B (en) | 1983-03-31 |
BE873263A (en) | 1979-05-02 |
CH637907A5 (en) | 1983-08-31 |
AU4305679A (en) | 1979-07-12 |
FR2413335B1 (en) | 1983-03-11 |
DK1078A (en) | 1979-07-03 |
FI63559C (en) | 1983-07-11 |
JPS6218497B2 (en) | 1987-04-23 |
PT68984A (en) | 1979-01-01 |
IE47772B1 (en) | 1984-06-13 |
IT1109909B (en) | 1985-12-23 |
FI784052A (en) | 1979-07-03 |
DK143938C (en) | 1982-04-19 |
ATA936978A (en) | 1991-11-15 |
NL185716B (en) | 1990-02-01 |
NL7900010A (en) | 1979-07-04 |
SE432417B (en) | 1984-04-02 |
NO144205B (en) | 1981-04-06 |
NO784417L (en) | 1979-07-03 |
SE432417C (en) | 1988-05-29 |
JPS54101922A (en) | 1979-08-10 |
NL185716C (en) | 1990-07-02 |
NO144205C (en) | 1981-07-15 |
DE2856206C2 (en) | 1988-02-25 |
IT7919016A0 (en) | 1979-01-02 |
DK143938B (en) | 1981-11-02 |
AT394709B (en) | 1992-06-10 |
GB2011379B (en) | 1982-06-30 |
ES476530A1 (en) | 1979-05-16 |
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