Gas odorization method

Information

  • Patent Grant
  • 7108803
  • Patent Number
    7,108,803
  • Date Filed
    Wednesday, August 4, 1999
    25 years ago
  • Date Issued
    Tuesday, September 19, 2006
    18 years ago
Abstract
A mixture of acrylic acid and nitrogen compounds is particularly adapted to achieve a sulfur-free odorization of a gas.
Description
FIELD OF THE INVENTION

The present invention relates to the odorization of gas.


Town and coke-oven gases obtained by thermal processes contained intensely odoriferous components and therefore had a strong intrinsic odor, so that escaping gas could be readily detected.


BACKGROUND OF THE INVENTION

Because of its origin (natural gas) and a relatively high degree of purity, the gas used nowadays in the public network is in itself virtually odorless; if leakages are not noticed in good time, explosive gas/air mixtures with a high hazard potential quickly form. For safety reasons, gas is therefore odorized by adding odorants. For example, in Germany it is stipulated that all gases which do not have sufficient intrinsic odor and are distributed in the public gas supply (DVGW-Arbeitsblatt [Worksheet] G 260) are odorized in accordance with DVGW-Arbeitsblatt [Worksheet] G 280; DVGW=Deutscher Verein des Gas-und Wasserfaches e.V. [German Association on Gas and Water], Eschborn. These odorizing compositions are detectable even when highly diluted and, because of their extremely unpleasant odor, act, as is desired, as a warning signal for people. In Germany, approximately 90% of service gas is currently odorized with tetrahydrothiophene (THT) (12–25 mg/m3); in addition, odorization using mercaptans or thioethers is also customary.


THT and mercaptans are highly suitable for reliable odorization of gas. However, in the context of treating the environment with more respect, it is to be noted that during the combustion of such odorized gases, sulfur dioxide forms as combustion product—only in small amounts at each individual combustion site, but, viewed on a countrywide scale, in amounts of a few hundred tons per year. It would be desirable to overcome this disadvantage; however, a number of requirements have to be satisfied:

  • 1. The odor must be unpleasant and unmistakable (odors from kitchens and homes are excluded). It must act as a warning signal for people who smell escaped gas.
  • 2. Everybody with an average sense of smell and average physiological condition must be able to detect the odor.
  • 3. The warning odor stage (=average odor intensity) must be achieved before the ignition limit or a kinetic carbon monoxide content is reached.
  • 4. The odorizing composition must be as nontoxic as possible and must not form any toxic combustion products.
  • 5. The odorizing composition must have high volatility and evaporate leaving as little residue as possible.
  • 6. A suitable odorizing composition must not condense at winter temperatures, nor separate, nor adhere to metallic pipes.
  • 7. The odorizing composition must combust without leaving a residue.
  • 8. The odorizing composition must be storage-stable and chemically resistant to the gas and to the plants. It must not promote corrosion, nor attack customary seals.


Attempts have already been undertaken to provide new gas odorizing compositions. Thus, the following, for example, have been proposed:

    • alkyl acrylates, vinyl or alkyl ethers and mixtures thereof (JP 76-7481),
    • n-valeric acid, optionally in combination with ethyl acrylate and/or triethylamine (JP 76-34 841),
    • mixtures of sulfur compounds and aliphatic aldehyde (JP 78-35 562),
    • cycohexene (JP 83-42 235),
    • norbornene derivatives (JP 87-1998) and
    • saturated ethers, saturated esters, and mixtures thereof with mercaptans.


SUMMARY OF THE INVENTION

It has now been found that, by additions of


A. acrylic C1–C12-, preferably C1–C8-alkyl, esters,


B. nitrogen compounds and optionally


C. antioxidants


progressively odorized gas is obtained which largely combines the desired properties. The novel odorizing composition can be added to the gas in the same order of magnitude as sulfur-containing compounds and does not produce corrosion-promoting products upon combustion.







DETAILED DESCRIPTION OF THE INVENTION

The acrylic esters A include methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate, n-butyl acrylate, isobutyl acrylate, tert-butyl acrylate, pentyl acrylate, hexyl acrylate, heptyl acrylate, octyl acrylate and dodecyl acrylate. In a preferred embodiment, mixtures of acrylic C1–C6-alkyl esters are used as component A; a particularly preferred combination comprises methyl acrylate and ethyl acrylate alongside one another. The acrylate mixtures can contain the lower and the higher esters in each case in the weight ratio of from 9:1 to 1:9, preferably 7:3 to 3:7.


Preferred nitrogen compounds B include primarily compounds

    • with a flash point above 20° C., preferably above 40° C. (measured in accordance with ISO 2719),
    • with a molecular weight of from 80 to 160, preferably 110 to 145,
    • with a boiling point of from 90 to 210, preferably 110 to 165° C.


The nitrogen compounds B include, for example,


lactones, such as caprolactone


nitriles, such as 2-nonenenitrile and compounds of the formula




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where

  • R1 to R4, independently of one another, are hydrogen or C1–C4-alkyl, preferably methyl or ethyl.


Preferred compounds (I) are e.g. 2-methylpyrazine, 2,3-dimethylpyrazine, 2,6-dimethylpyrazine, 2,3,5-trimethylpyrazine, tetramethylpyrazine, 2-ethylpyrazine, 2,3-diethylpyrazine, 5,2-methylethylpyrazine, 2,3-methylethylpyrazine, 5,2,3-methyldiethylpyrazine and 3,5,2- and 3,6,2-dimethylethylpyrazine, 2,3-methylethylpyrazine and tetramethylpyrazine are preferred.


The nitrogen compounds B can be used in amounts of from 1 to 100, preferably 30 to 100, in particular 10 to 50, parts by weight per 1 000 parts by weight of A.


To protect against undesired oxidation, the odorizing compositions may comprise antioxidants, as are described, for example, in Römpp-Lexikon Chemie Version 1.3. Preferred antioxidants include butylhydroxyanisole, ionol=tert-butylhydroxytoluene, hydroquinone monomethyl ether and α-tocopherol.


The antioxidants C are preferably used in amounts of from 0.01 to 5, in particular 0.05 to 2, especially 0.1 to 1, parts by weight per 1 000 parts by weight of A.


Preferred gas odorizing compositions can, for example, have the following compositions:


EXAMPLE 1

















Ethyl acrylate
600 g



Methyl acrylate
360 g



5,2,3-Methyldiethylpyrazine
 39 g



Ionol
 1 g










EXAMPLE 2

















Ethyl acrylate
535 g



Methyl acrylate
400 g



2-Methylpyrazine
 64 g



Ionol
 1 g










EXAMPLE 3

















Ethyl acrylate
320 g



Methyl acrylate
637 g



3,5(6),2-Dimethylethylpyrazine
 42 g



Ionol
 1 g










EXAMPLE 4

















Ethyl acrylate
460 g



Methyl acrylate
460 g



2,6-Dimethylpyrazine
 79 g



Ionol
 1 g










EXAMPLE 5

















Ethyl acrylate
520 g



Methyl acrylate
459 g



2,3,5-Trimethylpyrazine
 20 g



Ionol
 1 g










EXAMPLE 6

















Ethyl acrylate
885 g



Methyl acrylate
100 g



2,3-Methylethylpyrazine
 14 g



Ionol
 1 g










EXAMPLE 7

















Ethyl acrylate
700 g



Methyl acrylate
274 g



2,3-Dimethylpyrazine
 25 g



Ionol
 1 g










EXAMPLE 8

















Ethyl acrylate
350 g



Methyl acrylate
600 g



Tetramethylpyrazine
 49 g



Ionol
 1 g










EXAMPLE 9

















Ethyl acrylate
144 g



Methyl acrylate
800 g



2-Ethylpyrazine
 56 g










EXAMPLE 10

















Ethyl acrylate
615 g



Methyl acrylate
300 g



5,2-Methylethylpyrazine
 85 g










EXAMPLE 11

















Ethyl acrylate
320 g



Methyl acrylate
649 g



3,5(6),2-Dimethylethylpyrazine
 15 g



2,3-Dimethylethylpyrazine
 15 g



Ionol
 1 g










EXAMPLE 12

















Ethyl acrylate
120 g



Methyl acrylate
807 g



2-Ethylpyrazine
 30 g



5,2-Methylethylpyrazine
 42 g



Ionol
 1 g










EXAMPLE 13

















Ethyl acrylate
520 g



Methyl acrylate
434 g



2,6-Dimethylpyrazine
 20 g



2,3-Methylethylpyrazine
 25 g



Ionol
 1 g










EXAMPLE 14

















Ethyl acrylate
320 g



Methyl acrylate
633 g



2,3-Diethylpyrazine
 34 g



2,3-Methylethylpyrazine
 12 g



Ionol
 1 g










EXAMPLE 15

















Ethyl acrylate
759 g



Methyl acrylate
200 g



2-Methylpyrazine
 30 g



Tetramethylpyrazine
 10 g



Ionol
 1 g









Claims
  • 1. A method of imparting odor to an odorless combustible gas, said method comprising: adding to said odorless combustible gas
  • 2. A combustible gas comprising: 1) an odorless gas; and2) an odorizing composition comprising:A. a mixture of two acrylic C1–C12-alkyl esters, wherein the weight ratio of the two acrylic esters is 9:1 to 1:9,B. at least one N compound with a boiling point of from 90 to 210° C. and a molecular weight of from 80 to 160 and optionallyC. an antioxidant, wherein components A and B are odorants and are added to said combustible gas in an amount effective to act as a warning signal to warn of presence of said combustible gas in an enclosed space before an ignition limit of said combustible gas in said enclosed space is reached, and wherein said components A and B are substantially sulfur-free.
  • 3. The method according to claim 1, wherein said at least one N compound is of the formula:
  • 4. The method according to claim 1, wherein said at least one N compound is present in an amount of from 1 to 100 parts by weight per 1,000 parts by weight of said Component A.
  • 5. The method according to claim 1, wherein at least said antioxidant is used in an amount of from 0.01 to 5 parts by weight per 1,000 parts by weight of said Component A.
  • 6. The method according to claim 1, wherein said odor imparting components that are added to said combustible gas are non-corrosive.
  • 7. The gas according to claim 2, wherein said at least one N compound is of the formula:
  • 8. The gas according to claim 2, wherein said at least one N compound is present in an amount of from 1 to 100 parts by weight per 1,000 parts by weight of said Component A.
  • 9. The gas according to claim 2, wherein at least said antioxidant is used in an amount of from 0.01 to 5 parts by weight per 1,000 parts by weight of said Component A.
  • 10. The gas according to claim 2, wherein said odor imparting components that are added to said combustible gas are non-corrosive.
Priority Claims (1)
Number Date Country Kind
198 37 066 Aug 1998 DE national
PCT Information
Filing Document Filing Date Country Kind 371c Date
PCT/EP99/05639 8/4/1999 WO 00 3/12/2001
Publishing Document Publishing Date Country Kind
WO00/11120 3/2/2000 WO A
US Referenced Citations (4)
Number Name Date Kind
3620982 Grossman Nov 1971 A
4487613 Yoshida et al. Dec 1984 A
5321005 Mookherjee et al. Jun 1994 A
6296889 Ott et al. Oct 2001 B1
Foreign Referenced Citations (6)
Number Date Country
48-79804 Oct 1973 JP
76007481 Mar 1976 JP
51 034841 Sep 1976 JP
78035562 Sep 1978 JP
83042235 Sep 1983 JP
87001998 Jan 1987 JP