NO130048B - - Google Patents

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Info

Publication number: NO130048B
Authority: NO; Norway
Prior art keywords: machine according; concrete; feeding belt; wall; container
Prior art date: 1970-12-15

Application number

NO04610/71*[A

Other languages

English (en)

Norwegian (no)

Inventor

S Nilsson

Original Assignee

Nilcon Ab Ing Firman

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.)

1970-12-15

Filing date

1971-12-14

Publication date

1974-07-01

1971-12-14 Application filed by Nilcon Ab Ing Firman filed Critical Nilcon Ab Ing Firman

1974-07-01 Publication of NO130048B publication Critical patent/NO130048B/no

Links

238000000034 method Methods 0.000 claims description 8
239000000203 mixture Substances 0.000 claims description 8
238000004519 manufacturing process Methods 0.000 claims description 4
239000000758 substrate Substances 0.000 claims 4
230000007423 decrease Effects 0.000 claims 2
238000005056 compaction Methods 0.000 claims 1
230000006835 compression Effects 0.000 claims 1
238000007906 compression Methods 0.000 claims 1
238000007493 shaping process Methods 0.000 claims 1
238000009751 slip forming Methods 0.000 claims 1
SPJMAPNWDLIVRR-UHFFFAOYSA-M sodium;3-chloro-2-phenylphenolate Chemical compound [Na+].[O-]C1=CC=CC(Cl)=C1C1=CC=CC=C1 SPJMAPNWDLIVRR-UHFFFAOYSA-M 0.000 claims 1
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 24
150000001875 compounds Chemical class 0.000 description 14
JZUFKLXOESDKRF-UHFFFAOYSA-N Chlorothiazide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC2=C1NCNS2(=O)=O JZUFKLXOESDKRF-UHFFFAOYSA-N 0.000 description 13
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
150000003839 salts Chemical class 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 8
235000019256 formaldehyde Nutrition 0.000 description 7
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
239000002253 acid Substances 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 6
230000001882 diuretic effect Effects 0.000 description 6
229930040373 Paraformaldehyde Natural products 0.000 description 5
-1 alkali metal salts Chemical class 0.000 description 5
IHJCXVZDYSXXFT-UHFFFAOYSA-N chloraminophenamide Chemical compound NC1=CC(Cl)=C(S(N)(=O)=O)C=C1S(N)(=O)=O IHJCXVZDYSXXFT-UHFFFAOYSA-N 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
229960002155 chlorothiazide Drugs 0.000 description 4
SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 4
239000000155 melt Substances 0.000 description 4
230000001452 natriuretic effect Effects 0.000 description 4
241000282472 Canis lupus familiaris Species 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
208000004880 Polyuria Diseases 0.000 description 3
241000700159 Rattus Species 0.000 description 3
NKDDWNXOKDWJAK-UHFFFAOYSA-N dimethoxymethane Chemical compound COCOC NKDDWNXOKDWJAK-UHFFFAOYSA-N 0.000 description 3
239000002934 diuretic Substances 0.000 description 3
238000001704 evaporation Methods 0.000 description 3
230000008020 evaporation Effects 0.000 description 3
229920002866 paraformaldehyde Polymers 0.000 description 3
235000011121 sodium hydroxide Nutrition 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
239000000571 coke Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
230000029142 excretion Effects 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
239000012530 fluid Substances 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
WMFOQBRAJBCJND-UHFFFAOYSA-M lithium hydroxide Inorganic materials [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
239000011707 mineral Substances 0.000 description 2
235000010755 mineral Nutrition 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000011591 potassium Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
JVMPQYRPGCRZQH-UHFFFAOYSA-N 3-pentyl-4h-1$l^{6},2,4-benzothiadiazine 1,1-dioxide Chemical compound C1=CC=C2NC(CCCCC)=NS(=O)(=O)C2=C1 JVMPQYRPGCRZQH-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
208000029422 Hypernatremia Diseases 0.000 description 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
206010029164 Nephrotic syndrome Diseases 0.000 description 1
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
230000001154 acute effect Effects 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 1
MTHSVFCYNBDYFN-UHFFFAOYSA-N anhydrous diethylene glycol Natural products OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
230000037396 body weight Effects 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
239000003792 electrolyte Substances 0.000 description 1
MVEAAGBEUOMFRX-UHFFFAOYSA-N ethyl acetate;hydrochloride Chemical class Cl.CCOC(C)=O MVEAAGBEUOMFRX-UHFFFAOYSA-N 0.000 description 1
239000008098 formaldehyde solution Substances 0.000 description 1
125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
239000004312 hexamethylene tetramine Substances 0.000 description 1
235000010299 hexamethylene tetramine Nutrition 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
210000003734 kidney Anatomy 0.000 description 1
230000002045 lasting effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
210000004185 liver Anatomy 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
229910052987 metal hydride Inorganic materials 0.000 description 1
150000004681 metal hydrides Chemical class 0.000 description 1
229910000000 metal hydroxide Inorganic materials 0.000 description 1
150000004692 metal hydroxides Chemical class 0.000 description 1
239000008267 milk Substances 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
239000012452 mother liquor Substances 0.000 description 1
208000009928 nephrosis Diseases 0.000 description 1
231100001027 nephrosis Toxicity 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
235000016709 nutrition Nutrition 0.000 description 1
230000035764 nutrition Effects 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
NTTOTNSKUYCDAV-UHFFFAOYSA-N potassium hydride Chemical compound [KH] NTTOTNSKUYCDAV-UHFFFAOYSA-N 0.000 description 1
229910000105 potassium hydride Inorganic materials 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000007787 solid Substances 0.000 description 1
210000002700 urine Anatomy 0.000 description 1

Classifications

- B—PERFORMING OPERATIONS; TRANSPORTING
- B28—WORKING CEMENT, CLAY, OR STONE
- B28B—SHAPING CLAY OR OTHER CERAMIC COMPOSITIONS; SHAPING SLAG; SHAPING MIXTURES CONTAINING CEMENTITIOUS MATERIAL, e.g. PLASTER
- B28B1/00—Producing shaped prefabricated articles from the material
- B28B1/08—Producing shaped prefabricated articles from the material by vibrating or jolting
- B28B1/084—Producing shaped prefabricated articles from the material by vibrating or jolting the vibrating moulds or cores being moved horizontally for making strands of moulded articles

Landscapes

Engineering & Computer Science (AREA)
Manufacturing & Machinery (AREA)
Chemical & Material Sciences (AREA)
Ceramic Engineering (AREA)
Mechanical Engineering (AREA)
Devices For Post-Treatments, Processing, Supply, Discharge, And Other Processes (AREA)
On-Site Construction Work That Accompanies The Preparation And Application Of Concrete (AREA)
Press-Shaping Or Shaping Using Conveyers (AREA)
Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Manufacturing Of Tubular Articles Or Embedded Moulded Articles (AREA)

NO04610/71*[A 1970-12-15 1971-12-14 NO130048B (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
SE1695670		1970-12-15

Publications (1)

Publication Number	Publication Date
NO130048B true NO130048B (de)	1974-07-01

Family

ID=20303048

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO04610/71*[A NO130048B (de)	1970-12-15	1971-12-14

Country Status (18)

Country	Link
JP (1)	JPS5417766B1 (de)
AT (1)	AT318458B (de)
BE (1)	BE775319A (de)
CA (1)	CA946593A (de)
CH (1)	CH537263A (de)
CS (1)	CS159298B2 (de)
DE (1)	DE2152124B2 (de)
DK (1)	DK126976B (de)
ES (2)	ES398005A1 (de)
FI (1)	FI52676C (de)
FR (1)	FR2118494A5 (de)
GB (1)	GB1337298A (de)
HU (1)	HU171636B (de)
IL (1)	IL38322A (de)
IT (1)	IT940056B (de)
NL (1)	NL158424B (de)
NO (1)	NO130048B (de)
ZA (1)	ZA718140B (de)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB2128654A (en) *	1982-10-12	1984-05-02	Balfour Beatty Ltd	Wall panel
IT1195098B (it) *	1986-07-11	1988-10-12	Russo A & C Sas	Impianto per la produzione su pista di pannelli alveolari in cemento armato precompresso o parzialmente precompresso o con armatura lenta estesa alle superfici inferiore e superiore ed alle costole e prodotto derivato
FR2671119B1 (fr) *	1990-12-28	1993-04-09	Saret France	Elements de construction en beton, precontraint, du type predalles, installation et procede pour leur fabrication.
ES2155293B1 (es) *	1997-02-04	2001-12-16	Extremadura 2000 De Estructura	Procedimiento de fabricacion de placas pretensadas tipo pi por extrusion.

1971
- 1971-10-18 CA CA125,319A patent/CA946593A/en not_active Expired
- 1971-10-19 GB GB4847071A patent/GB1337298A/en not_active Expired
- 1971-10-19 AT AT902971A patent/AT318458B/de not_active IP Right Cessation
- 1971-10-20 DE DE2152124A patent/DE2152124B2/de active Granted
- 1971-10-27 IT IT70522/71A patent/IT940056B/it active
- 1971-10-29 DK DK529171AA patent/DK126976B/da unknown
- 1971-10-30 CH CH1574271A patent/CH537263A/de not_active IP Right Cessation
- 1971-11-03 FI FI713135A patent/FI52676C/fi active
- 1971-11-12 BE BE775319A patent/BE775319A/xx unknown
- 1971-11-14 NL NL7115634.A patent/NL158424B/xx unknown
- 1971-11-17 JP JP9157371A patent/JPS5417766B1/ja active Pending
- 1971-12-01 FR FR7143960A patent/FR2118494A5/fr not_active Expired
- 1971-12-06 ZA ZA718140A patent/ZA718140B/xx unknown
- 1971-12-08 IL IL38322A patent/IL38322A/en unknown
- 1971-12-10 HU HU71NI00000143A patent/HU171636B/hu unknown
- 1971-12-14 NO NO04610/71*[A patent/NO130048B/no unknown
- 1971-12-14 CS CS869071A patent/CS159298B2/cs unknown
- 1971-12-15 ES ES398005A patent/ES398005A1/es not_active Expired
- 1971-12-15 ES ES398004A patent/ES398004A1/es not_active Expired

Also Published As

Publication number	Publication date
SU438162A3 (ru)	1974-07-30
DE2152124C3 (de)	1974-09-19
GB1337298A (en)	1973-11-14
FR2118494A5 (de)	1972-07-28
ES398004A1 (es)	1974-07-01
HU171636B (hu)	1978-02-28
BE775319A (fr)	1972-03-01
NL158424B (nl)	1978-11-15
ES398005A1 (es)	1974-07-01
DK126976B (da)	1973-09-10
JPS5417766B1 (de)	1979-07-03
CA946593A (en)	1974-05-07
AT318458B (de)	1974-10-25
FI52676C (fi)	1977-12-01
CH537263A (de)	1973-05-31
DE2152124B2 (de)	1974-02-14
AU3490371A (en)	1973-05-03
FI52676B (de)	1977-08-01
DE2152124A1 (de)	1972-07-20
ZA718140B (en)	1972-08-30
NL7115634A (de)	1972-06-19
IL38322A0 (en)	1972-02-29
IT940056B (it)	1973-02-10
CS159298B2 (de)	1974-12-27
IL38322A (en)	1974-12-31

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SU488408A3 (ru)	1975-10-15	Способ получени замещенных 3-(2-4фенил-1-пиперазинил-этил)-индолинов или их солей, или их четвертичных аммониевых солей
NO138408B (no)	1978-05-22	Forbindelse for anvendelse som utgangsmateriale for fremstilling av 1-(4-metzyl-6-metoksy-2-pyrimidinyl)-3-metyl-5-metoksypyrazol, og fremgangsmaate for fremstilling av forbindelsen
PT100097A (pt)	1993-04-30	Novos agentes terapeuticos constituidos por derivados de quinolina e processo para a sua preparacao
NO137093B (no)	1977-09-19	Fremgangsm}te til fremstilling av 2,4-diamino-5-benzylpyrimidiner
NO150553B (no)	1984-07-30	Oppblaasbar baat
NO136574B (de)	1977-06-20
US2597445A (en)	1952-05-20	Nu-alkylamino-methyl-phenyl-propane and method of preparing same
NO150281B (no)	1984-06-12	Analogifremgangsmaate ved fremstilling av nye, terapeutisk aktive 3,4,5,6-tetrahydro(1,3)thiazolo(3,4-a)isokinolinderivater
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Wibaut et al.	1939	On the reactivity of the bromine atoms in brominated pyridines. the formation of 2, 6‐diamino‐4‐bromopyridine by the action of ammonia on 2, 4, 6‐tribromopyridine
US2741615A (en)	1956-04-10	N-substituted dihydrodesoxynorcodeine compounds
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KR820001715B1 (ko)	1982-09-21	치환된 2-페닐이미노-이미다졸리딘의 제조방법