IP Library Patent Application 18294009
Patent Application
App. No. 18/294,009

Method for the Processing and Transport of Hexane-1,6-Diamine or Pentane-1,5-Diamine

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Quick Facts
Patent No.
US None
App. No.
18/294,009
Abstract

The invention relates to a method for the processing and transport of hexane-1,6-diamine or pentane-1,5-diamine comprising the steps of: a) Providing a first composition including 60 to 98 wt.-% water and 2 to 40 wt.-% hexane-1,6-diamine or pentane-1,5-diamine, b) partially removing water from the first composition by distillation at a first production location, whereby a second composition is generated, said second composition including the hexane-1,6-diamine or pentane-1,5-diamine and 1 wt.-% to 35 wt.-% water, and c) transporting said second composition during a span of time t from the first production location to a second production location, wherein the span of time t including times for optional temporary storage is at least 6 h.

Claims (32)

1 . A method for the processing and transport of hexane-1,6-diamine or pentane-1,5-diamine comprising the steps of:

a) providing a first composition including 60 to 98 wt.-% water and 2 to 40 wt.-% hexane-1,6-diamine or pentane-1,5-diamine;

b) partially removing water from said first composition by distillation at a first production location, whereby a second composition is generated, said second composition including the hexane-1,6-diamine or pentane-1,5-diamine and 1 wt.-% to 35 wt.-% water; and

c) transporting said second composition during a span of time t from the first production location to a second production location, wherein the span of time includes times for optional temporary storage of at least 6 h.

2 . The method according to claim 1 , wherein the first composition includes 2 to 40 wt.-% hexane-1,6-diamine.

3 . The method according to claim 1 , wherein the first composition includes 2 to 40 wt.-% pentane-1,5-diamine.

4 . The method according to claim 1 , wherein the first composition provided in step a) is obtained by recycling polyurethanes, polythiourethanes, polyureas, polyisocyanurates and/or polyamides.

5 . The method according to claim 1 , wherein the first composition provided in step a) is obtained by biotechnological production of the diamine.

6 . The method according to claim 1 , wherein the first composition includes ≥3 wt.-% and ≤35 wt.-% hexane-1,6-diamine or pentane-1,5-diamine.

7 . The method according to claim 1 , wherein the water content of the first composition is ≥62 wt.-% and ≤95 wt.-%.

8 . The method according to claim 1 , wherein the water content of the second composition is in the range from 2 wt.-% to 27 wt.-% based on the entire second composition.

9 . The method according to claim 1 , wherein the transport takes place in vessels selected from the group consisting of transport containers, tank wagons and tankers.

10 . The method according to claim 1 , wherein the span of time t is at least 24 h.

11 . A method for producing a polyamide or an aliphatic diisocyanate comprising the steps of:

a) providing a first composition including 60 to 98 wt.-% water and 2 to 40 wt.-% hexane-1,6-diamine or pentane-1,5-diamine;

b) partially removing water from said first composition by distillation at a first production location, whereby a second composition is generated, said second composition including the hexane-1,6-diamine or pentane-1,5-diamine and 1 wt.-% to 35 wt.-% water; and

c) transporting said second composition during a span of time t from the first production location to a second production location, wherein the span of time includes times for optional temporary storage of at least 6 h;

d) optionally further purifying the second composition at the second production location, thus generating a third composition;

and either

e) phosgenating the second and/or the optionally obtained third composition at the second production location so that hexane-1,6-diamine or pentane-1,5-diisocyanate is generated;

or

f) polycondensing the second and/or the optionally obtained third composition at the second production location so that a polyamide based on hexane-1,6-diamine or pentane-1,5-diamine is generated;

or

g) converting the second and/or the optionally obtained third composition with a dicarboxylic acid to the diamine-dicarboxylic acid salt.

12 . The method according to claim 5 , wherein the biotechnological production of the diamine is by fermentation of suitable precursor compounds.

13 . The method according to claim 6 , wherein the first composition includes ≥5% wt.-% and ≤25 wt.-% hexane-1,6-diamine or pentane-1,5-diamine.

14 . The method according to claim 13 , wherein the first composition includes ≥7 wt.-% and ≤22 wt.-% hexane-1,6-diamine or pentane-1,5-diamine.

15 . The method according to claim 7 , wherein the water content of the first composition is ≥65 wt.-% and ≤90 wt.-%.

16 . The method according to claim 15 , wherein the water content of the first composition is ≥75 and ≤88 wt.-%.

17 . The method according to claim 8 , wherein the water content of the second composition is in the range from 5 wt.-% to 20 wt.-% based on the entire second composition.

18 . The method according to claim 10 , wherein the span of time t is at least 168 h.

19 . The method according to claim 18 , wherein the span of time t is at least 336 h.

Assignments (4)
SECURITY INTEREST Recorded Feb 10, 2026
From: GENOMATICA, INC.
To: AGAIN BIO APS
Reel/Frame 074708/0001 →
SECURITY INTEREST Recorded Dec 9, 2025
From: GENOMATICA, INC.
To: NOVO HOLDINGS A/S, AS COLLATERAL AGENT
Reel/Frame 073915/0027 →
SECURITY INTEREST Recorded Jun 2, 2025
From: GENOMATICA, INC.
To: OXFORD FINANCE LLC
Reel/Frame 071471/0770 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2024
From: MERKEL, MICHAEL
To: COVESTRO DEUTSCHLAND AG; GENOMATICA, INC.
Reel/Frame 067222/0543 →