PL75836B2 - - Google Patents

Download PDF

Info

Publication number
PL75836B2
PL75836B2 PL15669572A PL15669572A PL75836B2 PL 75836 B2 PL75836 B2 PL 75836B2 PL 15669572 A PL15669572 A PL 15669572A PL 15669572 A PL15669572 A PL 15669572A PL 75836 B2 PL75836 B2 PL 75836B2
Authority
PL
Poland
Prior art keywords
skeins
dibromovolanthrone
hours
urea
sodium acetate
Prior art date
Application number
PL15669572A
Other languages
Polish (pl)
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.)
Filing date
Publication date
Application filed filed Critical
Priority to PL15669572A priority Critical patent/PL75836B2/pl
Publication of PL75836B2 publication Critical patent/PL75836B2/pl

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Description

Wyfarbowanie prowadzi sie w temperaturze 60°C przez 30 minut. Po tym czasie dodaje sie roztwór (0,3 g hydrosulfitu w 5 ml wody destylowanej), temperature kapieli podnosi sie do 80°C i ogrzewa sie zanurzone motki mieszajac co jakis czas przez dalsze 30 minut. Nastepnie motki po wypraniu suszy sie na powietrzu. Motki sa wybarwione na kolor ciemnozielony. Celem uzyskania czerni nalezy poddac wybarwione motki kapieli utleniaja¬ cej (np. w roztworze podchlorynu).Przyklad II. W kolbie okraglodennej o pojemnosci 250 ml zaopatrzonej w chlodnice powietrzna umieszcza sie 9 g dwubromowiolantronu o zawartosci czystego dwubromowiolantronu 95%. Nastepnie dodaje sie 9 g mocznika i 4,5 g octanu sodowego oraz 0,01 g sproszkowanej miedzi metalicznej. Calosc ogrzewa sie na lazni olejowej w temperaturze 145-155°C przez 2 godziny. Podczas reakcji nastepuje lekkie spienienie njasy reakcyj¬ nej. Po uplywie 2 godzin do goracej mieszaniny reakcyjnej dolewa sie 60 ml wody destylowanej i calosc poddaje sie saczeniu, przemywa sie porcjami 4 razy po 30 ml goracej wody. Uzyskana wydajnosc produktu wynosi 6,7 g tj. 93,9% w stosunku do uzytego dwubromowiolantronu i 98,5% w stosunku do zawartosci dwubromowiolan¬ tronu.Otrzymany barwnik o wzorze sumarycznym C34 H16 N2 02 jest czarnym proszkiem o temperaturze rozkladu ponad 465°C.Otrzymane wybarwienie koloru ciemnozielonego na motkach bawelnianych potwierdza bardzo wysoki stopien czystosci otrzymanego produktu. PL PLThe dyeing is carried out at 60 ° C for 30 minutes. After this time, a solution (0.3 g of hydrosulfite in 5 ml of distilled water) is added, the bath temperature is raised to 80 ° C and the submerged skeins are heated with agitation at intervals for a further 30 minutes. The skeins are then dried in the air after washing. Skeins are colored dark green. To obtain blackness, the dyed skeins should be treated with an oxidizing bath (eg in a hypochlorite solution). Example II. In a 250 ml round bottom flask equipped with air coolers are placed 9 g of dibromoviolanthrone containing 95% pure dibromoviolanthrone. Then 9 g of urea and 4.5 g of sodium acetate and 0.01 g of powdered metallic copper are added. Everything is heated in an oil bath at 145-155 ° C for 2 hours. During the reaction, slight foaming of the reaction mixture occurs. After 2 hours, 60 ml of distilled water is poured into the hot reaction mixture and the whole is filtered, washed 4 times with 30 ml of hot water. The obtained product yield is 6.7 g, i.e. 93.9% in relation to the used dibromovolanthrone and 98.5% in relation to the content of dibromovolanthrone. The obtained dye with the formula C34 H16 N2 02 is a black powder with a decomposition temperature over 465 ° C. C. The obtained dark green color on the cotton skeins confirms a very high degree of purity of the obtained product. PL PL

Claims (1)

1. Zastrzezenie patentowe Sposób wytwarzania barwnika dwuaminowiolantronowego, znamienny tym, ze dwubromowiolantron pod¬ daje sie reakcji stapiania z mocznikiem i octanem sodowym w temperaturze najkorzystniej od 140 do 160°C przez okres 2 godzin wobec sproszkowanej miedzi metalicznej jako katalizatora. Prac. Poligraf. UP PRL. zam. 1670/74 naklad 120+18 Cena 10 zl PL PLClaim 1. A process for the preparation of a diamino-volanthrone dye, characterized in that dibromovolanthrone is fused with urea and sodium acetate at a temperature of preferably 140 to 160 ° C for a period of 2 hours in the presence of powdered metallic copper as the catalyst. Wash. Typographer. UP PRL. residing 1670/74 circulation 120 + 18 Price PLN 10 PL PL
PL15669572A 1972-07-14 1972-07-14 PL75836B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL15669572A PL75836B2 (en) 1972-07-14 1972-07-14

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL15669572A PL75836B2 (en) 1972-07-14 1972-07-14

Publications (1)

Publication Number Publication Date
PL75836B2 true PL75836B2 (en) 1974-12-31

Family

ID=19959364

Family Applications (1)

Application Number Title Priority Date Filing Date
PL15669572A PL75836B2 (en) 1972-07-14 1972-07-14

Country Status (1)

Country Link
PL (1) PL75836B2 (en)

Similar Documents

Publication Publication Date Title
US4009995A (en) Process for dyeing molded articles containing urea formaldehyde resin or melamine formaldehyde resin
PL75836B2 (en)
CH610593A5 (en) Process for preparing disperse dyes of the monoazo series
DE3071637D1 (en) Distyrylebenzenes,process for their preparation and their use for the optical brightening of organic materials,as well as detergent compositions, textile treating compositions and products for the after-treatment of laundry containing such distyrylbenzenes
EP0019702A3 (en) Distyrylebiphenyles, process for their preparation and their use for the optical brightening of organic materials, as well as detergent compositions, textile treating compositions and products for the after-treatment of laundry containing them
JPS6346193B2 (en)
JPS5634759A (en) Production of vat dyeing dyestuff
EP0156977A3 (en) Process for the preparation of a bleaching activator in granular form
CN113072439A (en) Clean process for synthesizing 1, 4-dihydroxy anthraquinone
SU462851A1 (en) The method of obtaining the final form of sulfur dyes
SU608866A1 (en) Two-phase suspension method of dyeing cellulose-containing textile material
SU445336A1 (en) Method of preparing black vat colour
US2445699A (en) Manufacture of 2-anthrahydroquinone-carboxylic acid
SU405939A1 (en) METHOD OF OBTAINING A SURFACE-ACTIVE
US1783137A (en) Process for manufacturing a green vat dyestuff from 1.12 perylene quinone
JP3210976B2 (en) Dyeing method with safflower and ranka powder
SU475791A3 (en) Method of imparting non-salability, non-shrinkage and bleaching of wool fiber
SU385520A1 (en)
SU382665A1 (en) WAY OF OBTAINING DISPERSE DYE
SU122227A1 (en) The method of obtaining vat dyes
SU1742380A1 (en) Method of preparing dyeing modified polyester fiber
KR810001683B1 (en) Silk thread dyeing method
SU1305221A1 (en) Method of dyeing cellulose-containing textile materials
PL56364B1 (en)
SU148377A1 (en) The method of obtaining colors and printing patterns on the fibers