CH164811A - Process for the production of a wetting agent for alkaline baths. - Google Patents
Process for the production of a wetting agent for alkaline baths.Info
- Publication number
- CH164811A CH164811A CH164811DA CH164811A CH 164811 A CH164811 A CH 164811A CH 164811D A CH164811D A CH 164811DA CH 164811 A CH164811 A CH 164811A
- Authority
- CH
- Switzerland
- Prior art keywords
- wetting agent
- production
- alkaline baths
- alkali
- alkaline
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 7
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 239000000080 wetting agent Substances 0.000 title description 5
- 239000003513 alkali Substances 0.000 claims description 5
- 239000010665 pine oil Substances 0.000 claims description 5
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 claims description 4
- 239000000126 substance Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 3
- -1 terpene alcohols Chemical class 0.000 description 3
- 235000007586 terpenes Nutrition 0.000 description 3
- 238000009736 wetting Methods 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- NNRLDGQZIVUQTE-UHFFFAOYSA-N gamma-Terpineol Chemical compound CC(C)=C1CCC(C)(O)CC1 NNRLDGQZIVUQTE-UHFFFAOYSA-N 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 238000009992 mercerising Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- 229930006727 (-)-endo-fenchol Natural products 0.000 description 1
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 1
- WUOACPNHFRMFPN-SECBINFHSA-N (S)-(-)-alpha-terpineol Chemical compound CC1=CC[C@@H](C(C)(C)O)CC1 WUOACPNHFRMFPN-SECBINFHSA-N 0.000 description 1
- RUJPNZNXGCHGID-UHFFFAOYSA-N (Z)-beta-Terpineol Natural products CC(=C)C1CCC(C)(O)CC1 RUJPNZNXGCHGID-UHFFFAOYSA-N 0.000 description 1
- IAIHUHQCLTYTSF-MRTMQBJTSA-N Fenchyl alcohol Chemical compound C1C[C@]2(C)[C@H](O)C(C)(C)[C@H]1C2 IAIHUHQCLTYTSF-MRTMQBJTSA-N 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- OVKDFILSBMEKLT-UHFFFAOYSA-N alpha-Terpineol Natural products CC(=C)C1(O)CCC(C)=CC1 OVKDFILSBMEKLT-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 1
- 229940116229 borneol Drugs 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000012084 conversion product Substances 0.000 description 1
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- IAIHUHQCLTYTSF-UHFFFAOYSA-N fenchyl alcohol Natural products C1CC2(C)C(O)C(C)(C)C1C2 IAIHUHQCLTYTSF-UHFFFAOYSA-N 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- XONPDZSGENTBNJ-UHFFFAOYSA-N molecular hydrogen;sodium Chemical compound [Na].[H][H] XONPDZSGENTBNJ-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- QJVXKWHHAMZTBY-GCPOEHJPSA-N syringin Chemical compound COC1=CC(\C=C\CO)=CC(OC)=C1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 QJVXKWHHAMZTBY-GCPOEHJPSA-N 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/144—Alcohols; Metal alcoholates
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/38—Oxides or hydroxides of elements of Groups 1 or 11 of the Periodic Table
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
- D06M13/248—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing sulfur
- D06M13/256—Sulfonated compounds esters thereof, e.g. sultones
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
- D06M13/282—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
- D06M13/288—Phosphonic or phosphonous acids or derivatives thereof
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatment Of Fiber Materials (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Netzmittels für alkalische Bäder. Es wurde gefunden, dass man zu einem wertvollen Netzmittel für alkalische Bäder gelangt, wenn man einen Terpenalkohol mit einem alkalibeständigen sulfonierten Fett körper vermischt.
Als Terpenalkohole lassen sich gesättigte wie ungesättigte Alkohole der Terpenreihe, wie a-, ss- und y-Terpineol, Terpineol-1, 2- Menthanol, Fenchylalkohol, Borneol und der gleichen verwenden. Es ist vorteilhaft, von natürlich anfallenden Mischungen, die solche Terpenalkohole in wesentlichen Mengen ent halten, auszugehen, beispielsweise von Pineöl.
Als alkalibeständige sulfonierte Fett körper kann man beispielsweise die Sulfonie- rungsprodukte von ungesättigten oder Oxy- gruppen enthaltenden Fettsäuren, deren Gly- ceriden oder Estern mit einwertigen Alko holen verwenden.
Derartige Produkte können beispielsweise erhalten werden durch Sulfo- nierung von höheren ungesättigten Fettsäuren und deren Umwandlungsprodukten, wie Ricinusöl, in Gegenwart -von sulfonierten aromatischen Karbonsäuren und -deren An hydriden, wovon das Verfahren der Schwei zer Patentschrift Nr. 146540 ein -Beispiel gibt.
Zur Herstellung des neuen Netzmittels kann man das neutralisierte Sulfierungsprö- dukt des Fettkörpers mit dem Terpenalkohol vermischen; man kann den letzteren aber auch vor dem Neutralisieren hinzufügen und die Mischung mit Alkalihydroxyden oder Alkalikarbonaten neutralisieren.
Das gemäss vorliegender Erfindung her gestellte Netzmittel erhöht die Netzfähigkeit von alkalischen Flotten in hervorragender Weise. Es eignet .sich insbesondere als Zusatz zu Mercerisierlaugen, wobei die Oberflächen spannung der Alkalihydroxydlösungen so stark herabgesetzt wird, dass man Rohware ohne vorherige Benetzung der - Mercerisätion unterwerfen kann. Man erzielt dabei in kür zester Zeit eine vollständige Schrumpfung -und ein Maximum an Glanz.
Beispiel: Ricinusöl wird in Gegenwart von Phthal- säureanhydrid-ss-sülfosäure nach einer Aus- führungsform- des Verfahrens der Schweizer Patentschrift Nr. 146540 mit Schwefelsäure sülfonisiert, neutralisiert und mit soviel Pine- öl versetzt, däss das Endprodukt bei einem Gehalt von .etwa- <B>30</B> % Fettsäure etwa 5 Pineöl enthält:
Man erhält ein klares<B>01,</B> das von Wasser leicht- zu einer beim Schütteln schäumenden Lösung aufgenommen wird.
Beim -Mercerisieren, beispielsweise von trockenem Rohzwirn, setzt man der Merceri- sierlauge (23;5%igeNatriumhydrogydlösunb) 5 % des beschriebenen Hilfsstoffes zu. Der. Mercersationsprözess verläuft darnach sehr rasch.
Die Netzwirkung der Mercerisierlauge, kann noch etwas erhöht- werden, wenn man dem sulfonierten Öl ausser 5 % Pineöl 2 Amylalkohol zusetzt.
Process for the production of a wetting agent for alkaline baths. It has been found that a valuable wetting agent for alkaline baths is obtained if a terpene alcohol is mixed with an alkali-resistant sulfonated fatty substance.
As terpene alcohols, saturated and unsaturated alcohols of the terpene series, such as α-, β- and γ-terpineol, terpineol-1,2-menthanol, fenchyl alcohol, borneol and the like can be used. It is advantageous to start from naturally occurring mixtures containing such terpene alcohols in substantial amounts, for example from pine oil.
The sulfonation products of unsaturated fatty acids or fatty acids containing oxy groups, their glycerides or esters with monovalent alcohols can be used as alkali-resistant sulfonated fatty substances.
Such products can be obtained, for example, by sulfonating higher unsaturated fatty acids and their conversion products, such as castor oil, in the presence of sulfonated aromatic carboxylic acids and their anhydrides, of which the process of Swiss Patent No. 146540 gives an example.
To produce the new wetting agent, the neutralized sulphonation product of the fatty substance can be mixed with the terpene alcohol; but you can also add the latter before neutralizing and neutralize the mixture with alkali hydroxides or alkali carbonates.
The wetting agent produced according to the present invention increases the wetting ability of alkaline liquors in an outstanding manner. It is particularly suitable as an additive to mercerising liquors, the surface tension of the alkali hydroxide solutions being reduced so much that raw materials can be subjected to mercerising without prior wetting. Complete shrinkage and maximum gloss are achieved in a very short time.
Example: Castor oil is sulphonized with sulfuric acid in the presence of phthalic anhydride-ss-sulphonic acid according to an embodiment of the process of Swiss patent specification No. 146540, neutralized and mixed with enough pine oil that the end product with a content of - <B> 30 </B>% fatty acid contains about 5 pine oil:
A clear 01 is obtained, which is easily absorbed by water to form a solution which foams when shaken.
When mercerizing, for example dry raw twine, 5% of the auxiliary substance described is added to the mercerizing liquor (23; 5% sodium hydrogen solution). The. The mercury process then proceeds very quickly.
The wetting effect of the mercerizing liquor can be increased somewhat if amyl alcohol is added to the sulfonated oil in addition to 5% pine oil.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH164811T | 1932-11-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH164811A true CH164811A (en) | 1933-10-31 |
Family
ID=4417757
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH164811D CH164811A (en) | 1932-11-26 | 1932-11-26 | Process for the production of a wetting agent for alkaline baths. |
| CH173382D CH173382A (en) | 1932-11-26 | 1933-12-09 | Process for the production of wetting agents for alkaline baths and wetting agent produced therefrom. |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH173382D CH173382A (en) | 1932-11-26 | 1933-12-09 | Process for the production of wetting agents for alkaline baths and wetting agent produced therefrom. |
Country Status (3)
| Country | Link |
|---|---|
| CH (2) | CH164811A (en) |
| FR (2) | FR763716A (en) |
| GB (1) | GB442047A (en) |
-
1932
- 1932-11-26 CH CH164811D patent/CH164811A/en unknown
-
1933
- 1933-11-13 FR FR763716D patent/FR763716A/en not_active Expired
- 1933-12-09 CH CH173382D patent/CH173382A/en unknown
-
1934
- 1934-12-06 FR FR45649D patent/FR45649E/en not_active Expired
- 1934-12-07 GB GB3522434A patent/GB442047A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR763716A (en) | 1934-05-04 |
| CH173382A (en) | 1934-11-30 |
| FR45649E (en) | 1935-11-02 |
| GB442047A (en) | 1936-01-31 |
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