US816457A - Blue fibrous material and process of dyeing same. - Google Patents
Blue fibrous material and process of dyeing same. Download PDFInfo
- Publication number
- US816457A US816457A US24463905A US1905244639A US816457A US 816457 A US816457 A US 816457A US 24463905 A US24463905 A US 24463905A US 1905244639 A US1905244639 A US 1905244639A US 816457 A US816457 A US 816457A
- Authority
- US
- United States
- Prior art keywords
- fibrous material
- blue
- dyeing
- blue fibrous
- dyeing same
- 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 - Lifetime
Links
- 238000004043 dyeing Methods 0.000 title description 2
- 239000002657 fibrous material Substances 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- FBEHFRAORPEGFH-UHFFFAOYSA-N Allyxycarb Chemical compound CNC(=O)OC1=CC(C)=C(N(CC=C)CC=C)C(C)=C1 FBEHFRAORPEGFH-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- -1 oXy Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B51/00—Nitro or nitroso dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Materials For Medical Uses (AREA)
Description
Application filedfebru To (all whom it UMZZ/ suite-aria:
Be it known that I, Vim-0e Ph. D., chemist, a ei' en Austrieliungery, res Main, Germany, have in. and useful hnprovemelns in Dyeing Blue, of which the specification,
I have found that by e: 'zing e in of alkylated dianiidobenzhyoiels end i oXy or para-amide dipheuylemin 21y derivatives new dyestufis of vivid him be obthined which are d inguished by t fastness to Washing, so soda, elkeli and acid even in the absence 0 i i It is known that tetren'iethyidiei zhydrol with acids yields beeutuu tinted salt-s deeoiorized by an excess L1). e On tannin-mordented cotton. or si 3 salts produce beautiful shades ness, however, and being re posed by soap, dilute alkali. (Compare Nietzki, One m. HI edition, pages iii.) stuffs obtained by this YIOL" w, must not be mistaken for the known ,1- the aikyleted (iliil'llidObGIlZlIFClIOiS question here of new eondensetieri II tetramethyldiemidobenzhy oxidized, no dyestufi is b dizing gem-oily or pare-amide d it by ltse e lwht grey 1s pee-d2 ever, the hydrol be mixer diphenvlsmin derivative din color and oxidized on t stugs of beautiful shades m ness are obtained. in e simiis in the derivatives of pareor y e1 diphenylemin-lihefm insten ee, pare-oxy-diphenyiamin, fHLlTlliFtBLm nylemin and their homolegues wi methyldiamidobenzhydrol and of! l lyted diemidobenzhydrols. The corr 111g methane derivatives, like tetra. i anudodlphenylmetheme, when oxidized on the fiber together with para emidoc ipheiiylemin also yield a blue dyestuil of the sat-in e excellent properties. This is due prob b l to the hydrol being first formed 7 the methane derivative, whereupon it; with p era-amidediphenylemin. Thus stance, ara-oxydiphenylemin and tet methyldiamldobenzhydi'ol yield e vivid vie- "is min and v I M tetrathe stL l The bodies to be a "products of the (TJ'DliCELlJlOIi ZOO
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24463905A US816457A (en) | 1905-02-07 | 1905-02-07 | Blue fibrous material and process of dyeing same. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24463905A US816457A (en) | 1905-02-07 | 1905-02-07 | Blue fibrous material and process of dyeing same. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US816457A true US816457A (en) | 1906-03-27 |
Family
ID=2884939
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US24463905A Expired - Lifetime US816457A (en) | 1905-02-07 | 1905-02-07 | Blue fibrous material and process of dyeing same. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US816457A (en) |
-
1905
- 1905-02-07 US US24463905A patent/US816457A/en not_active Expired - Lifetime
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