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A traditional specialty

for innovative cleaners


Hostapur SAS

Hostapur SAS
contents

Product profile

Physical and chemical properties

28

sythesis

Surface activity

30

Applications

12

Foaming power

31

Dishwashing liquids

15

Rheological properties

31

Detergents

18

pH stability

31

Household cleaners

21

Heat stability

31

Sanitary cleaners

22

Detergent action

31

Cosmetic hair and body care products

23

Solubilization

32

Industrial cleaners

26

Emulsifying action

32

Special technical sectors

27

Stability to hard water

32

Electrolyte stability

32

Chlorine-/oxidation stability

33

Enzyme stability

33

Synergistic interaction with soil release polymers

34

Solubility in water

35

Low-temperature properties

35

hostapur SAS

Toxicological and environmental properties

36

Technical Data

48

Toxicological profile

38

Summary of the properties of Hostapur SAS

49

Ecology

39

Physical/chemical data

50

Life cycle assessment

41

Ecological data

51

Processing

42

C-chain distribution

51

Transport

44

Registration status

51

Storage

44

Analysis

53

Conveying/mixing

46

Literature

53

Dilution

46

product range

55

Handling

47

Hostapur SAS

Product profile

hostapur SAS

Hostapur SAS A surfactant with


optimum application properties and
less impact on the environment
The demands imposed on surfactants have changed in the last few
decades. Not only is an optimum price-performance ratio expected,
but safety and impact on the environmental are also prime
considerations.
The secondary alkane sulphonate Hostapur SAS meets these
requirements in every respect. This surfactant has been
highly successful on the market for many years. To date, over
one million metric tonnes of Hostapur SAS have been produced
in our european facilities.
One of the reasons for this great success is the enhanced
environmental properties as shown by the life cycle assessment.
We are convinced that over the coming decades Hostapur SAS
will continue to maintain and expand its position as one of the
leading principal surfactants.
This brochure describes the specific properties and universal
uses of Hostapur SAS. Further information and individual advice
can be obtained.

Abbreviations

SAS

Secondary alkane sulphonate

LES

Lauryl ether sulphate

LAS

Linear alkylbenzene sulphonate

AES

Alkyl ether sulphate

LS

Lauryl sulphate

SRP

Soil release polymer

Hostapur SAS
Grades

Anionic surfactants for the detergent, chemical-technical and


cosmetic industries, based on secondary alkane sulphonate
sodium salt, starting product: n-paraffins.
Chemical structure

CH3 (CH2)m CH (CH2)n CH3


|

SO3- Na+

m + n = 10 14; the sulphonate group is distributed


over the carbon chain in such a way that it is mainly
the secondary carbon atoms that are substituted.
INCI name

Sodium C14-17 sec-Alkyl sulphonate


CAS numbers

97489-15-1; 85711-70-2; 85711-69-9,


USA: 68608-26-4; 68037-49-0
EINE CS/ELIN CS numbers

307-055-2; 288-331-9; 288-330-3

Commercially available grades


Active content

Appearance (25C)

Hostapur SAS 30

approx. 30%

clear faintly yellowish liquid

Hostapur SAS 60

approx. 60%

yellowish soft paste

Hostapur SAS 93

approx. 93%

yellowish waxy pellets

Hostapur SAS 93 G

approx. 93%

yellowish fine granules

hostapur SAS

The Hostapur SAS grades are noted for the following


specific application properties:
Very good solubility

Increases action of modern detergent additives,

spontaneous dissolving, e.g. when used as dishwashing liquids


good low-temperature properties

e.g. soil release polymers


Very good electrolyte compatibility

High wetting action

manufacture of heavy-duty detergents with high builder content

good drainage properties and rapid drying of dishes


Good skin compatibility
Pronounced foaming power

formulation of mild dishwashing liquids

high yield of the finished products in use


Possibility of combination with anionic,
Excellent grease- and soil-dispersing action

nonionic and amphoteric surfactants

development of finished products with defined and optimum


detergent, cleaning and degreasing action

versatility in formulation
synergistic effects in use
electrically neutral salts can be formed with cationic surfactants

Viscosity-depressing action

permits the formulation of flowable, highly concentrated


detergents and cleaners with low water content and without
solvents and preservatives; saves transport and packaging costs

Cost reduction

Outstanding enzyme compatibility

Surfactant of low aquatic toxicity with less

positive influence on enzyme stability

impact on the environment

possibility of manufacturing highly concentrated liquid cleaners


without hydrotropes

rapid biodegradation
Chemical stability over a wide pH range

formulation of alkaline cleaners with long storage stability


stability to oxidizing agents; intended for chlorine-containing
all-purpose cleaners

Range of grades

Hostapur SAS is available in liquid and paste as well as in pellet


and powder form
permits universal processing in all fields of use

Hostapur SAS
Synthesis

hostapur SAS

The synthesis of Hostapur SAS


by the Hoechst light/water process
yields detergent raw materials
of consistently high quality.
In this process the raw material
and energy consumption
as well as the emissions
are optimized at a minimum.

The secondary alkane


sulphonate Hostapur SAS
is synthesized
by sulphoxidation
of n-paraffins.1-6

Sulphoxidation, a basic reaction in aliphatic organic chemistry,


was discovered as early as 1940 by C. Platz at the Hchst site of
the former IG Farben AG 7, when n-paraffins were treated with
sulphur dioxide and oxygen and simultaneously exposed to
ultraviolet light. Since then the process has been developed into
the present Hoechst light/water process 811, which can be
described summarily by the following equation:

Substitution is done largely at the methylene groups; the terminal


methyl groups are considerably less reactive. 12 14
Besides the monosulphonates, smaller amounts of di- and
polysulphonates are also formed, see Technical data, page 48.

RH + 2SO2 + O2 + H2O RSO3H + H2SO4

Figure 1: Sulphoxidation process

The flow chart shows in diagrammatic form the industrial-scale production of Hostapur SAS.

SO3

O2

n-paraffin

reaction

n-paraffin

H2O

H2O

SAS-flakes 93%

rectification

H2O
separation

neutralisation

SAS- paste 60%

SO2

10

O2

n-paraffin

NaOH

hostapur SAS

The industrial-scale sulphoxidation of the n-paraffins by the


Hoechst light/water process is carried out in a multi-lamp reactor.
The gas mixture of SO2 and O2 is introduced by means of gas
injection equipment and on exposure to UV light produced in highpressure mercury lamps made of quartz glass, sulphoxidation of
the n-paraffins takes place in the presence of water. The reaction
gas is circulated. A compressor is needed for maintaining gas
circulation, as is a cooling system for adjusting the required
temperature. The reaction liquid is removed at the bottom of the
reactor and the product phase the lower phase is separated
in a separating system. The upper phase paraffin phase is cooled
and replenished with water and n-paraffin and then returned to
the reactor. After concentration of the product phase in a vacuum,
separation of the sulphuric acid and neutralization of the concentrate with sodium hydroxide solution, the remaining paraffin is
driven off with superheated steam. The distillate is again separated
in a separator and the paraffin phase is returned to the reaction.
The remaining melt is finally processed into pellets, Hostapur SAS
93, or into aqueous solutions, Hostapur SAS 60 or Hostapur SAS 30.
Very pale reaction products of high quality are obtained.
One characteristic of the process described is that no other
chemical auxiliaries, for example, solid catalysts or solvents, are
required. The n-paraffins used for synthesis are obtained as a
matter of course in the production of kerosene, and so Hostapur
SAS manufacture offers a useful outlet for this material. The
precise material flow and the energy balances are described in
section Life cycle assessment, page 41.

11

Hostapur SAS

ApplicationS

12

hostapur SAS

The Hostapur SAS grades are


principal surfactants with
excellent ecological, toxicological
and economic properties.
Because of their pronounced surface activity and
specific properties, they have a very wide range of uses.
Their major use is in dishwashing liquids, in which
Hostapur SAS has proved highly successful for several
decades. The Hostapur SAS grades are used as principal
surfactants in combination with other surfactants for
the manufacture of virtually all types of detergents and
cleaners for household and industrial use.

13

Most important uses for


Hostapur SAS

Dishwashing liquids

Standard dishwashing liquids


Dishwashing liquid concentrates

Laundry detergents

Liquid detergents
Detergent powders
Detergent pastes
Soaking agents

Household cleaners

All-purpose cleaners
Liquid metal/ceramic cleaner
Sanitary cleaners
Floor cleaners
Glass cleaners
Toilet freshener blocks

14

Cosmetic hair and


body care products

Shampoos
Showergels
Foam baths
Liquid soaps
Toothpastes

Industrial cleaners

Automotive cleaners
Metal degreasing agents
Alkaline rust removers
Hand cleaners

Special technical sectors

Antistatic agents for polyvinyl chloride,


polystyrene and polyethylene
Fire extinguishing foams
Emulsion polymerization
Textile and leather auxiliaries
Oilfield chemicals

hostapur SAS

Dishwashing
liquids

Consumers expect modern dishwashing liquids primarily to have


optimum cleaning action and safety in use, in other words good skin
compatibility, coupled with optimum environmental compatibility.

Hostapur SAS 60 is not preserved and, like Hostapur SAS 93, is


suitable for the manufacture of preservative-free preparations.

Another desirable feature is high yield, which can be achieved with


concentrates. Adequate foaming power in the presence of grease
and absence of streaks on dishes are taken for granted.

The low-temperature stability of the dishwashing liquids, for


example, at -5C, can be further improved by small additions of
OH-group-containing substances such as ethanol. An addition of
2% ethanol and 2% urea is recommended for concentrates with
about 40% active detergent.

Hostapur SAS as a principal surfactant in combination with amphoteric surfactants such as the alkyl amidobetaines and/or alkyl ether
sulphates and/or nonionic surfactants as co-surfactants enables
dishwashing liquids to be developed that meet the above-mentioned
requirements almost ideally.15 -20

pH adjustment is generally done with sodium hydroxide solution


or citric acid. When alkyl amidobetaines are used, an increase in
viscosity may possibly occur in the acid pH range.

The high solubility of Hostapur SAS enables highly concentrated


dishwashing liquids with good storage stability to be formulated
without the addition of cost-increasing solubilizers. The demand
for this product class is rising steadily.

If necessary, moisturizing agents can additionally be incorporated


in the formulation. Because of the good dermatological properties
of Hostapur SAS this is, however, not necessary in most cases.

Advantages of Hostapur SAS

These concentrates with a low water content offer primarily


economic advantages such as lower transport and packaging costs.
It is often possible to dispense with a preservative for these
concentrates. Guide Formulations are available.

in dishwashing liquids
Very good solubility and thus economizing on solubilizers
Very good rinsing action, rapid drainage, shine and rapid drying
Optimum cleaning and degreasing action with a low concent-

Preservation of formulations containing Hostapur SAS depends


foremost on the composition of the finished product in question.
Hostapur SAS is a rapidly biodegradable surfactant and must therefore be preserved if the finished formulations have a low application
concentration and a high water content. Most of the commercially
available preservatives are suitable for this purpose. A preservative
loading test must however always be carried out. Formulations
with a fairly high active detergent content, for example, over 40%,
usually do not need to be preserved.
Microbiological studies of Hostapur SAS as a function of the
concentration of active detergent showed that an inherently
bacteriostatic effect is displayed with concentrations as low as
about 40%. Therefore the sixty-percent commercial grade
15

ration of active detergent and thus high dishwashing efficiency


Creamy, fine-bubble foam, which can act as a soil- and

fat-suspending agent
Compatibility with anionic, nonionic and amphoteric surfactants.
As a result synergistic effects are often achieved
Faint inherent colour and therefore only small amounts of dye
are required if coloration is needed
Good skin compatibility, especially in combination with
other surfactants

Dishwashing
liquids

The skin compatibility and the foaming power can be optimized


by combining Hostapur SAS and alkyl ether sulphate, for example,
Genapol LRO or ZRO. In practice a mixture of about 3 to 4 parts
Hostapur SAS and about one part alkyl ether sulphate, relative to
100% active substance (ratio 3:1 or 4:1), has proved successful.

Figure 2: Viscosity of Hostapur SAS: alkyl ether sulphate mixtures


with the addition of ethanol and urea
100000

viscosity [mPas]

Of the numerous possibilities for combining Hostapur SAS with


surfactants that have a different chemical structure two-, threeand four-component combinations are described below by way of
example; these mixtures enable dishwashing liquids with tailormade properties to be developed.

10000

1000

100

10

This combination also enables liquid concentrates with about 40%


active detergent content to be formulated without the additional
use of a solubilizer. Moreover, with this concentration the mixture
of Hostapur SAS and alkyl ether sulphate is better and more rapidly
soluble in the dishwashing water than the individual components
separately.
The stability to hard water and the foaming power in hard water
are also optimized by the alkyl ether sulphate content. By adding
magnesium ions or other divalent metal ions to the Hostapur SAS:
alkyl ether sulphate mixture the foaming power can be further
improved, especially in the extremely low water hardness range.

10

40

A n 4 parts SAS: 1 part LES + 10% ethanol + 10% urea


B n 4 parts LAS: 1 part LES + 10% ethanol + 10% urea

Fig. 2 shows the viscosity at +20C as a function of the concentration of Hostapur SAS/alkyl ether sulphate mixtures with the
addition of ethanol and urea. This means that a 40% formulation
consisting of 32% Hostapur SAS and 8% lauryl ether sulphate
contains 4% ethanol and 4% urea.

A crucial parameter for the processing and use of dishwashing


liquids is rheology. The viscosity of the commercially available
products is about 400 to 700 mPas/20C. This viscosity can be
achieved easily with 5 to 7% sodium chloride in Hostapur SAS:
alkyl ether sulphate mixtures in the ratio 70:30, relative to 100%
active detergent, and a content of 12 to 15% active detergent in
the final formulation.
More highly concentrated Hostapur SAS: alkyl ether sulphate
mixtures with a 40% active detergent content can be adjusted
easily to viscosities suitable for practical purposes by incorporating
viscosity-depressing additives such as ethanol and/or urea,
as shown in fig. 2.
16

20
30
concentration c [%]

hostapur SAS

Figure 3: Mini-plate test of Hostapur SAS: alkyl ether sulphate (4:1 mixtures)

as a function of magnesium ion addition

water hardness: 0ppm CaCO3 (0d)

number of plates

15

When betaines are used, not only the dermatological properties but
also the rheological properties are improved. As a result additional
moisturizing agents and viscosifiers are often not required. 21
A fatty alcohol polyglycol ether content, as a function of the fatty
alcohol radical and the degree of ethoxylation, can produce an
increase in solubilizing and emulsifying action as well as better
wetting. These influence the cleaning effect to a marked degree
when the product is used. The pronounced solubilizing action of
Hostapur SAS can also obviate the need for special solubilizers
for slightly soluble perfume oils, and thus cut costs.

10

0
0

0.3

0.6
0.9
Mg++-concentration [%]

1.2

1.5

Finally, there is the possibility of combining the four surfactant


classes: alkane sulphonate, alkyl ether sulphate, betaine and fatty
alcohol polyglycol ether.

n concentration: 0.33 g a.s./L

The cleaning action can be tested in the mini-plate test on glass


plates soiled with grease or in the plate test. An example is given
in fig. 3.
Three-component mixtures can be formulated
with Hostapur SAS , alkyl ether sulphate and betaine
(alkyl dimethyl betaine or alkyl amidobetaine), for example,
mixed in the ratio 5:2:1 or 7:1:1, or
with Hostapur SAS , alkyl ether sulphate and nonionic fatty
alcohol polyglycol ethers.

17

In the aforementioned numerous possible combinations the


economical principal surfactant Hostapur SAS is used as the
main component. Depending on the mixing ratio, the application
properties of these combinations such as degreasing, low-temperature properties, foaming power, feel on the skin, rheology and
dermatology can be optimized. 22, 23

Detergents

Liquid detergents

Liquid detergents are a major field of application for Hostapur SAS


on account of its pronounced detergent properties.
The liquid detergents are divided below into light-duty liquids for
delicate wash and heavy-duty liquid detergents.
The market for heavy-duty liquid detergents is still fairly young
in Europe. In the USA the importance of these heavy-duty liquid
detergents is much greater. These liquid detergents contain an
average between 35 and 50% surfactants. In the USA the builders used are, for example, potassium tripolyphosphate and pyrophosphate and sodium citrate. In Europe, by contrast, phosphates
are largely notused. Moreover, in the USA, washing machines are
designed differently from those in Europe and the average washing temperatures are lower than 30C. The US formulations also
do not contain any bleaching agents because these are mostly used
separately.

As with the dishwashing liquids, when Hostapur SAS is used as the


principal surfactant, for example, instead of linear alkyl benzene
sulphonate, considerable savings of solubilizer such as ethanol
can be achieved. Optimum liquid detergents without builders and
having very good detergent action, solubility and stability contain
as principal components Hostapur SAS, readily water-soluble
higher-ethoxylated fatty alcohols and potassium or triethanolamine
coconut soap; the anionic surfactant content of the total active
detergent is generally one-third.25

In Europe the liquid detergents used have a different structure.


They generally consist of a mixture of anionic and nonionic
surfactants with soap in approximately the same ratio. In addition
they contain solubilizers such as ethanol, propylene glycol and/
or xylene sulphonate, possibly enzymes, optical brighteners and
chelating agents. 15 24
If enzymes are used in the formulations, Hostapur SAS offers better
enzyme compatibility than most of the anionic surfactants such as
linear alkyl benzene sulphonate or alkyl sulphate.

18

hostapur SAS

If builders are also incorporated in the liquid detergents, it is advantageous to use freely soluble surfactants such as Hostapur SAS.
A further beneficial property of Hostapur SAS is its good electrolyte
compatibility, in other words good compatibility with the builders.

Advantages of Hostapur SAS in heavy-duty

The liquid light-duty detergents are used at temperatures up to


a maximum of 60C. Hostapur SAS as a principal surfactant can
be combined in amounts of up to 40% with alkyl ether sulphates,
nonionic surfactants, amphoteric surfactants and/or soap.

manufactured

and light-duty liquid detergents


Better solubility in water than linear alkyl benzene sulphonate
High solubility, enabling highly concentrated detergents to be
Hydrotropes can be reduced in quantity or omitted
Good detergent action
Good dispersion and solubilization of the soil,

oil and fat particles


Another possibility of formulating with Hostapur SAS is to develop
highly viscous to gel-like detergents with special rheological
properties in use. Hostapur SAS permits a high surfactant
concentration and rapid dissolving in use. Hostapur SAS permits
a high surfactant concentration and rapid dissolving in use.

Pronounced foaming power in the presence of soil and fat


Good compatibility with electrolytes, which enables the
hydrotropes to be reduced or even eliminated
Good calcium ion tolerance
Saving on enzymes
Synergistic effects with soil release polymers

Looking ahead, the demand for liquid detergents will undoubtedly


continue to increase within the detergent market in Europe. This
applies particularly to products that have an active detergent
content of 50 percent and above. They thus meet the requirements
for low-energy manufacture, high efficiency coupled with easy low
metering and less impact on the environment. Detergents with high
active substance concentrations can be developed without difficulty
with Hostapur SAS.

19

Good dermatological properties

Detergents

detergent
powders

Hostapur SAS can also be used to manufacture the various powder


detergent types. The excellent solubility and the solubilizing
properties lower the viscosity of the slurry. This brings a number
of major advantages, especially substantial energy savings and
capacity increases in the manufacture of detergent powders by the
hot spraying process.

Advantages of Hostapur SAS in

Fig. 4 shows an example of typical viscosity/solids content curves,


determined on rehydrated tower powders. The powders each contained 9% Hostapur SAS (100%) or linear alkyl benzene sulphonate
(100%). The substantially lower viscosity of the Hostapur SAS
containing slurry is clearly discernible; measured in the Brabender
Plastograph, model PI 3S. 26

Energy and time saving

Powder-type light-duty detergents contain 10 to 15% Hostapur


SAS, relative to 100% active detergent, in combination with small
amounts of soap and fatty alcohol polyglycol ethers.

Lower slurry viscosity


Higher solid content

Increase of spraying capacity


Reduction of hydrolysis of sodium tripolyphosphate

due to less water content

Figure 4: Relative viscosities of detergent slurries as a function


of the solids content and the type of sulphonate
600
rel. viscosity [scales*]

Powder-type heavy-duty detergents can contain between 6 and


10% Hostapur SAS, relative to 100% active detergent, in combination with fatty alcohol polyglycol ethers and soap as surfactant
components.

detergent powders

500
400
300
200
100
0
0

55

60
solid content [%]

n SAS
n LAS
* measured with Brabender Plastograph

20

hostapur SAS

65

Household cleaners

Liquid all-purpose
cleaners and
Liquid metal/
ceramic cleaner

Liquid all-purpose cleaners

Liquid metal/ceramic cleaner

Liquid all-purpose cleaners are the predominant household


cleaners because of their ease of metering and wide range of uses.
In general they are adjusted to a fairly low concentration of active
detergent. Owing to the electrolyte content, for example, sodium
chloride or sodium carbonate, solubility problems and thus cloudiness may occur. Hostapur SAS, on the other hand, has specific
advantages for the formulation of all-purpose cleaners because of
itsexcellent solubility and electrolyte compatibility. 27, 28

Liquid metal/ceramic cleaner usually contains a high abrasive


content. The insoluble components are dispersed in the aqueous
surfactant phase. To prevent the solid particles from settling,
firstly abrasives with as small a particle size as possible are used
and secondly a fairly high viscosity is employed.

This also applies to the incorporation of fairly large amounts of


water-soluble active detergents or to the formulation of fairly highly
concentrated finished products. The latter can be produced with
Hostapur SAS without any great problems; an addition of solvent
such as butyl diglycol is often advantageous here. Abrasives such
as calcium carbonate can also be combined in high amounts with
Hostapur SAS. For the effective use of liquid all-purpose cleaners,
high fat-dissolving power and soil-dispersing power are of crucial
importance. Hostapur SAS brings these advantages in combination
with other components.
In addition the product has an excellent wetting action even at low
temperatures. This is particularly important for rapid cleaning; and
equally for a largely streakfree and residue-free removal of dirt.

By combining Hostapur SAS with other surfactants, for example,


with Genapol UD 030, it is often possible without adding
viscosifiers to increase the viscosity to a level where settling of
the abrasive particles is prevented or reduced.
The usually thixotropic formulations display advantageous
properties in use: during storage the viscosity is high and when
subject to shear stress during application the metal cleaner
becomes less viscous, in other words it flows readily from the
bottle and can be spread easily over the surface to be treated.
Depending on its composition, the liquid metal cleaner can be
applied to stainless steel, chromium, copper and brass surfaces.
Besides a mild and gentle cleaning action, consumers expect
above all a shiny finish and a water-repellent effect. The finished
products are, however, intended to be suitable as widely as possible
for the cleaning of glass ceramics. Here, too, rapid wetting of
the surface to be cleaned, as made possible by Hostapur SAS,
is important.

Advantages of Hostapur SAS in


liquid all-purpose cleaners
Advantages of Hostapur SAS in
Excellent wetting action: Rapid distribution over the dirty,

liquid metal/ceramic cleaner

greasy surfaces to be cleaned


Electrolyte compatibility: Reduction in or elimination

Advantageous rheological properties when applied

of hydrotropes

Stabilization of the abrasives

Strong degreasing and cleaning action: Largely

Good wetting action increases efficiency

streak-free surfaces

Good grease-dissolving power

Good solubility Manufacture of highly concentrated

all-purpose cleaners
Good skin compatibility
21

Household cleaners

Sanitary cleaners

Sanitary cleaners are used chiefly for the easy and economical
cleaning of bathrooms and toilets. They are intended to remove all
traces of lime, dirt and soap rapidly. Furthermore, it is often desired
to remove dark mould patches on joints, tiles and shower curtains.
The current sanitary cleaners are adjusted either to an acid or an
alkaline pH. In general these products are expected to have an
antimicrobial or disinfectant action as well, which can be achieved
by special additives such as active chlorine (hypochlorite) hydrogen
peroxide or by acids.
Surfactants with good wetting action provide the cleaning action.
Owing to its chemical structure (C-S bond to the sulphonate group),
Hostapur SAS has good stability to oxidizing agents and is stable in
both the acid and the alkaline pH ranges. This stability to reducing
and oxidizing agents makes Hostapur SAS a preferred surfactant
for sanitary cleaners.

Of special importance is the stability of the oxidizing agents used in


the individual surfactant systems.
The allround cleaners for baths are intended to be effective at
fairly low surfactant concentrations. As a result of the pronounced
wetting and cleaning action of Hostapur SAS, this is also achieved
according to the EC recommendation at anionic surfactant concentrations between 5 and 15% in the finished product.
The chemical stability of Hostapur SAS also enables it to be used
in toilet freshener blocks.

Advantages of Hostapur SAS in sanitary cleaners


Chemical stability to oxidizing agents
Stability in the acid and alkaline pH ranges
Good wetting power and thus increase in effectiveness
Better chlorine stability than other surfactants

22

hostapur SAS

Cosmetic

hair and body care


products

In cosmetic preparations Hostapur SAS has proved successful


particularly as a co-surfactant on account of its productspecific
properties. This applies especially to the combination with alkyl
ether sulphates in the manufacture of hair and body care products.29
Compared to alkyl ether sulphates, Hostapur SAS has a stronger
cleaning and degreasing action. The viscosity depressing property
of the secondary alkane sulphonate also limits the concentration
used in the fairly high-viscosity cosmetic hair and body care
products. Apart from exceptions, mixtures with a higher content
of alkyl ether sulphate are therefore used.
Guide values for the mixing ratios are as follows:
For finished products with a content over 12% active detergent:
70 parts ether sulphate to 30 parts Hostapur SAS.
For finished products with less than 12% active detergent
the mixing ratio should be: 80 parts ether sulphate to 20 parts
Hostapur SAS.
The mixing ratios are calculated on 100% active substance.

The viscosity can be adjusted with sodium chloride and/or


ammonium chloride and/or magnesium chloride very economically. Similarly, fatty acid alkanolamides and fatty alcohol polyglycol
ethers with a low degree of ethoxylation such as Genapol L-3 in
combination with the above-mentioned electrolytes can be used.
Fatty acid polyglycol esters or special cellulose ethers can also
be used to increase viscosity.
Fig. 5 shows the viscosity curves of Hostapur SAS (SAS): alkyl ether
sulphate (AES) mixtures with the addition of different electrolytes;
magnesium chloride performs particularly well. The viscosity rises
parallel to an increasing amount of alkyl ether sulphate.
A combination of alkyl ether sulphate, alkyl amidobetaine and
Hostapur SAS, for example, in the mixing ratio 6:2:2, can
bring advantages in respect of rheology, foaming properties
and dermatological properties.

Figure 5: Viscosity increase of alkyl ether sulphate/Hostapur SAS mixtures

as a result of additions of electrolytes (5%)


7000

viscosity [mPas]

6000
5000
4000
3000
2000
1000
0
7:3

6:4

5:5
SAS: AES mixture

n NaCl 10% a.s.


n KCl 15% a.s.
n NaCl 15% a.s.
n MgCl2 10% a.s.
n NH4OH 15% a.s. n MgCl2 15% a.s.

23

4:6

3:7

Cosmetic

hair and body care


products

By adding Hostapur SAS to liquid hair and body care products the
low-temperature cloud point as a function of the active detergent
content and the mixing ratio can be lowered by about 4 to 7C.
This is a particular advantage also for preparations containing
pearlizing agents. Fig. 6 illustrates the good influence of Hostapur
SAS on the low-temperature properties of the surfactant mixtures.

of the mixing ratio


+15

temperature [C]

The addition of Hostapur SAS enables hair shampoos with special


effects to be developed. The stronger degreasing action of Hostapur
SAS makes it possible to increase the cleaning action, for example,
in mixtures with alkyl ether sulphates. This is an advantage in
formulating low-cost effective shampoos for greasy hair.
The possibility is also afforded of manufacturing singleapplication
shampoos, which can obviate the need for washing a second time.

Figure 6: Low temperature cloud and clear points as a function

Shampoo concentrates with a high active detergent content can


also be formulated with Hostapur SAS in combination with
other surfactants. Here, the viscosity-depressing property of
Hostapur SAS is an advantage in formulation; in other words,
viscosity depressing additives such as ethanol and glycols can
largely be omitted.

+10
+5
0
-5
-1

Hair shampoos

0:10

2:8

4:6

6:4

8:2

10:0

SAS: AES mixture


n cloud point

n clear point

Special emulsifiers or solubilizers are needed to solubilize slightly


soluble perfume oils. Owing to the pronounced solubilizing action
of Hostapur SAS, the use of these auxiliaries is often unnecessary.
The flash foam required for use, especially in the presence of dirt
and grease, can also be increased by the Hostapur SAS content in
the formulations.

Last but not least, Hostapur is suitable for the manufacture of


special clean shampoos, which enable hair setting products or
highly substantive cationic polymers to be washed out of hair.
Shower gels

The universally usable shower gels are generally used for


cleaning the skin and hair at the same time. Flash foam formation
is particularly important in this application. With the partly use
of Hostapur SAS a fine-bubble foam and rapid spread of the shower
gel over the skin and hair can be achieved, as a function of the
concentration used.

The numerous uses of Hostapur SAS in cosmetic preparations are


described briefly as follows:

24

hostapur SAS

Foam baths

Advantages of Hostapur SAS in

Foam baths are used in extremely diluted concentrations in the


bath water; the active detergent content in the bath water is
0.002%. The finished products are therefore often adjusted to an
active detergent content of, for example, 50%. When the usual
surfactants such as alkyl ether sulphates and alkyl amidobetaines
are used, a gel that is slightly soluble in the bath water is usually
produced in this concentration range. By adding Hostapur SAS,
the solubility in water is improved dramatically. At the same time
beneficial rheological properties such as flowability at room
temperature are achieved. Moreover, it is not necessary to add
the commonly used solubilizers.

cosmetic preparations

Liquid soaps

Liquid soaps have become established as an alternative to


conventional bar soaps in the body care product sector, above
all because of their ease of use. Since the hands are, generally
speaking, fairly dirty, a strong cleaning action is required.
By using Hostapur SAS, this effect can be achieved easily.
Soaps

By adding, for example, 1 to 3% Hostapur SAS to the soap


formulation, processing can be facilitated and dispersion of the
dyes used can be improved. To a certain extent the amount
of the expensive C12 fatty acid can be reduced.
Emulsions

By adding small amounts of Hostapur SAS to emulsions, especially


oil-in-water emulsions, the spontaneity of emulsion formation can
be improved during manufacture. Moreover, finer distribution of
the emulsified droplets is achieved.
Toothpastes

Hostapur SAS can also be used in toothpastes as an alternative to


the lauryl sulphate sodium salt often employed as a foamer in dental
care products. Advantages are the good cleaning action as well as
the good electrolyte compatibility and dispersing action

25

Lowering of the raw material costs by partial replacement

of other principal surfactants


Improvement in low-temperature stability
Manufacture of highly concentrated formulations
Improvement in spontaneous solubility in water
Reduction in solubilizers, especially with concentrates
Foam stabilization
Increased cleaning action by varying the Hostapur SAS:
alkyl ether sulphate mixing ratio

Industrial

cleaners

High-pressure cleaners

Advantages of Hostapur SAS in

These cleaners are in many cases adjusted to an alkaline pH with


sodium hydroxide and sodium metasilicate. Hostapur SAS has
optimum foaming and cleaning action in this pH range as well.

Industrial cleaners

Automotive cleaners

Good compatibility with all types of electrolytes

Hostapur SAS is used as a principal surfactant in car shampoos


for private use and for commercial car washes. Equally, acid,
alkaline or neutral cleaners can be formulated with Hostapur SAS
for buses, railway trucks and lorries. The high cleaning action
of the secondary alkane sulphonate in particular is of great
importance here. Furthermore, the foaming properties and the
associated soil-and oil-suspending power play a major role in
effective use. The concentration of Hostapur SAS used, calculated
on 100%, is generally between 2 and 5%. Hostapur SAS can
however also be used with fatty alcohol polyglycol ethers in an
approximate mixing ratio of 3:1.

Excellent wetting power

High stability in a broad pH range (acid and alcaline)

and oxidation agents

Strong degreasing and cleaning effects


Good dispersion and solubilization of fat, soil, and pigments
High solubility and a good cold stability

Alkaline rust removers

The pH stability in the presence of potassium hydroxide solution


makes Hostapur SAS in amounts of 1 to 2% ideal for use in these
products.
Hand cleaners

Hand cleaners are used in industrial plants and workshops


for cleaning very dirty hands. To increase the cleaning action,
mechanically effective substances such as wood flour, soda,
sodium sulphate or polymer powder are used. Hostapur SAS
in amounts of 10 to 50% can be used as the active detergent.
The dispersion action and degreasing power of this surfactant
is an advantage for this application.
Cleaners for dairies and butchers shops

Hostapur SAS can be used for manufacture of cleaners for butchers


shops and milking machines because of its excellent cleaning and
degreasing power.

26

hostapur SAS

Special technical sectors

Hostapur SAS has many uses


in the technical sector.

Antistatic agents for polyvinyl chloride, polystyrene and polyethylene Plastics mostly have the undesirable property of
accumulating a static charge. Surfactants such as Hostapur SAS
form on the surface of the polymers a mono- or multi-molecular
film, which increases the conductivity with atmospheric moisture.
It is often possible to incorporate Hostapur SAS in the polymer
compound, for example, in the case of polyvinyl chloride.
This also applies to polystyrene and styrene copolymers and to
polyethylene.
Fire extinguishing foams

The pronounced flash foaming power of Hostapur SAS can be


used in combination with other surfactants very effectively to
formulate fire extinguishing agents.
Emulsion polymerization

Secondary alkane sulphonates have been used successfully for


decades in the emulsion polymerization of vinyl chloride.
Hostapur SAS has proved successful both as an emulsifier in
continuous and discontinuous processes and for the stabilization
of the latex following polymerization by the nucleation process;
in the latter process polymerization is carried out with only a
low emulsifier concentration and the dispersion is stabilized
subsequently by adding suitable emulsifiers. Hostapur SAS is
noted for its good dispersibility, which is evidenced by good
stability of the latex to mechanical stress and good process control
(little tendency for deposits to form in the reaction vessel).
Owing to the absence of double bonds, the emulsifier does not
act as a radical interceptor. This ensures a readily reproducible
reaction course and results in end products with good heat
stability because of the lower demand for persulphate (radical
forming agent) and the lower tendency to block polymerization
(no reaction between the emulsifier and the reaction partners).
The low salt content of Hostapur SAS also has a positive influence
on the heat stability of the end product.

are generally used. The soaps have the advantage over the
synthetic anionic emulsifiers that the polymer can be precipitated
by acidification or addition of salt and the fatty or resin acid
remaining in the product serves as a plasticizer at the same time.
One evident disadvantage of the soaps is the instability of the latex
(coagulation on slight change in pH and contamination, low
resistance to fillers) and poorer chemical and heat stability.
For these reasons the synthetic emulsifiers are increasingly gaining
ground, particularly for special products, for example, the carboxylated butadiene copolymers (for carpet backcoating, for papermaking, adhesives etc). Because of its constant quality and low salt
content, Hostapur SAS is highly suitable for this application.
Textile and leather auxiliaries

Owing to its chemical stability and very good wetting action,


Hostapur SAS can be used in the manufacture of synthetic fibres
and in the finishing of textile fibres, for example, as an antistatic
agent. 30 Other uses for the secondary alkane sulphonate are cotton
scouring, mercerizing and carbonization and the preparation of
leather fatliquors.
Oilfield chemicals

Hostapur SAS is also used successfully in the tertiary recovery of oil.

Advantages of Hostapur SAS for


special technical sectors
Excellent antistatic effect for polyethylene, polystyrene

and polyvinyl chloride


High foam stability and flash foaming power in combination
with co-surfactants
Good emulsifier for the emulsion polymerization in continuous
and discontinuous processes
High wetting action in textile and leather auxiliaries

for manufacture and finishing of textile fibres


In the manufacture of butadiene copolymers, butadienestyrene
and butadiene-acrylonitrile latices, soaps (fatty soaps, resin soaps)
27

Special additive with high heat and electrolyte stability

for the tertiary recovery of oil

Hostapur SAS

Physical and
chemical properties

28

hostapur SAS

The secondary alkane sulphonates


have a number of specific physical
and chemical properties
because of their structure.31 51
These properties are dependent
on the chain length of the paraffin
used. Hostapur SAS with paraffin
radicals between 14 and 17 carbon
atoms has optimum surface-active
and chemical properties, which
are described below.

29

Hostapur SAS

surface activity

pH ranges. The excellent wetting power in low concentrations


at low temperatures is a noteworthy feature.

Micelle formation

There are extensive studies of the surface-active properties of


secondary alkane sulphonates. 52, 53 It is interesting to note that
surfactants with a central functional group form micelles from
comparatively few surfactant molecules.54 For Hostapur SAS the
critical micelle concentration CM is about 2 x 10-3 molL -1 or
0.6 gL-1 at 20C. The structure of the micelles is spherical.

Fig. 8 shows the wetting action of Hostapur SAS as a function of


the concentration and temperature.
The superior wetting power of Hostapur SAS compared with linear
alkyl benzene sulphonate (LAS), lauryl ether sulphate (LE S) and
lauryl sulphate (LS) is shown in fig. 9.

Interfacial tension

The interfacial tension with decane as the other phase is about


4.6 mNm-1, measured on a 1% aqueous Hostapur SAS solution.

Figure 8: Wetting power of Hostapur SAS in accordance with DIN 53901


100

Surface tension

The surface tension of Hostapur SAS (100% active substance),


measured by the du Noy method at 25C, as a function of
the concentration, is shown in fig. 7.
Wetting action

Hostapur SAS is a rapidly wetting surfactant. This gives rise to


advantages in practical use in all cleaners. This applies particularly
to use in dishwashing liquids and all-purpose cleaners. The
excellent wetting action extends over a wide temperature range,
not only in a neutral medium but also in the alkaline and acid

wetting time [s]

80
60
40
20
0
0.25

0.75

concentration c [g/L]
n 20C

Figure 7: Surface tension of Hostapur SAS (25 C)

0.5

n 50C

n 70C

Figure 9: Wetting power of various surfactants in accordance with DIN 53901

80

60

wetting time [s]

surface tension [mN/m]

90
70

50
40
30

70
60
50
40
30
20
10
0

0.001

30

0.01
0.1
concentration [g/L]

10

SAS
LAS
C surfactant 0.1% a.s., temperature 37C,
water hardness: 268ppm CaCO3 (15d), pH 7
hostapur SAS

AES

LS

Hostapur SAS

chemical properties

Foaming power

Hostapur SAS has good foaming power, which is very pronounced,


especially in soft water. Flash foam is a characteristic property
of the secondary alkane sulphonates. An increase in foaming
properties, especially in hard water, can be achieved, for example,
by a combination of Hostapur SAS with an alkyl ether sulphate in
the ratio 4:1. Figs. 10 and 11 below demonstrate the foaming power
of Hostapur SAS in soft and hard water.

The flow properties of Hostapur SAS 30 and pastegrade Hostapur


SAS 60 are of importance particularly for transport and conveying.
The flow diagrams are given in section Conveying/mixing.
pH stability

The Hostapur SAS grades are stable in the acid and in the alkaline
pH range.
Heat stability

The good foaming properties of the Hostapur SAS/alkyl ether


sulphate mixtures are clearly discernible.

Aqueous solutions of Hostapur SAS are stable up to temperatures


of about 100C. The Hostapur SAS 93 pellets have a softening point
of about 40C and become liquid when the temperature rises to
about 140C. At temperatures above 140C, the surface of the
Hostapur SAS 93 melt should be covered with an inert gas blanket
such as nitrogen.

Rheological properties

The viscosity of the aqueous Hostapur SAS solutions rises only


slightly up to about 30% active detergent. Above 30%, however,
a rapid rise in the inhomogeneous paste region can be observed.
The low-concentration aqueous Hostapur SAS solutions exhibit
Newtonian flow.

Detergent action

The good soil removal power of Hostapur SAS is not appreciably


reduced by water hardness salts. The builders used in practice
increase the cleaning effect.

Figure 10: Foaming power of Hostapur SAS in distilled water

Figure 11: Foaming properties of Hostapur SAS in hard water

by the ROSS-MILES method

300

300

250

250
foam height [mm]

foam height [mm]

by the ROSS-MILES method

200
150
100
50
0

150
100
50
0

0.002

n AES

n SAS

0.006

0.03
0.1
concentration c [%]

n AES: SAS 7:3 n SAS: AES 4:1

water hardness 0ppm CaCO3 (0d), temperature 37C


31

200

0.3

1.0

0.002

n AES

n SAS

0.006

0.03
0.1
concentration c [%]

n AES: SAS 7:3 n SAS: AES 4:1

water hardness 357ppm CaCO3 (20d), temperature 37C

0.3

1.0

Hostapur SAS

chemical properties

Solubilization

Stability to hard water

The good solubilizing power of Hostapur SAS towards hydrophobic


oils and fats is characteristic of this type of surfactant. In practical
use in cleaners, this means increased degreasing and often a saving
of solubilizers, for example, for perfumes. The solubilizing effect
rises with the surfactant concentration, the temperature and often
also with the electrolyte content of the solution. Solubilization in
the Hostapur SAS solution can also be increased and speeded up by
mechanical means and lengthy stirring.

Hostapur SAS has a stability number of 3 in accordance with the


DIN 53905 test. Accordingly, Hostapur SAS is a surfactant with
moderate stability to hard water.

Using the solubilization of isopropyl myristate as an example, fig. 12


illustrates that Hostapur SAS has greater solubilizing power than
alkyl ether sulphate.

Electrolyte stability

The stability to hard water of Hostapur SAS can be improved


markedly by combining it with alkyl ether sulphates. As fig. 13
shows, a mixture of 4 parts Hostapur SAS (SAS) and 1 part lauryl
ether sulphate (LE S) reaches an optimum value of 75.

Hostapur SAS has only slight sensitivity to electrolytes. The viscosity of the aqueous solutions is increased only slightly by additions of
electrolyte such as sodium chloride or sodium sulphate.

Emulsifying action

Secondary alkane sulphonates also display good emulsifying action.


As co-emulsifiers, they are suitable for the manufacture of liquid
and cream oil-in-water emulsions. Concentrations as low as under
1% bring spontaneous emulsion formation in manufacture and an
improvement in emulsion stability. Moreover, finer distribution of
the emulsified droplets is possible. The emulsifying action
as a dishwashing liquid test is described by D. Miller. 55

Figure 12: Solubilization of isopropyl myristate by Hostapur SAS :

Figure 13: Stability to hard water of Hostapur SAS and of mixtures with lauryl
ether sulphate determined in accordance with DIN 53905

alkyl ether sulphate (LES ) as a function of the mixing ratio


5

80

wetting time [s]

wetting time [s]

4
3
2
1
0

60

40

20

0
0:10

2:8

4:6

6:4

8:2

10:0

SAS

SAS:LES mixture
n 15% a.s.

32

n 10% a.s.

n 5% a.s.

hostapur SAS

LES

SAS:LES 4:1

Hostapur SAS has excellent chlorine stability compared with many


other surfactants. In combination with amine oxides, a synergistic
effect is observed; in other words, the mixture has a higher stability
than the individual surfactants alone. Hostapur SAS is therefore the
ideal surfactant for formulating hypochlorite-containing cleaners,
whether used alone or in combination with amine oxides.
As illustrated in fig. 14, the chlorine content falls fairly little in the
presence of Hostapur SAS as a function of the storage time. The
stability was determined on a solution with 2.5% active detergent
in each case.
Enzyme stability

The stability of enzymes such as protease (e.g. Savinase, manufactured by Novozymes) in the presence of Hostapur SAS is shown
in fig. 15 as a function of the storage time. It is clearly evident
that after 7 days only a slight fall in enzyme activity (80%) can
be observed in the case of Hostapur SAS. Hostapur SAS is a more
enzyme compatible anionic surfactant than most anionic surfactants commonly used in liquid laundry detergent applications
(e.g. linear alkyl benzene sulphonate).

Figure 14: Chlorine stability in the presence of Hostapur SAS, amine oxide and

a mixture of Hostapur SAS/amine oxide

The residual activities after 7 days storage at 25C are shown in


fig. 16. Here too the good effect of Hostapur SAS on the stability
of the enzymes is confirmed both in the case of proteases and of
lipases.

Figure 15: Compatibility of Hostapur SAS with protease


100
residual activity [%]

Chlorine-/ oxidation stability

80
60
40
20
0
0

time [days]
n LAS
n SAS
c savinase 0.3%, c surfactant 3.0g/L,
water hardness 179ppm CaCO3 (10d), temperature 25C

Figure 16: Compatibility of Hostapur SAS with protease and lipase


100
residual activity [%]

residual activity [%]

100
80
60
40

80
60
40
20

20
0
0

SAS
2.5% SAS

2.5% amine oxide

after n 6 weeks, n after 12 weeks, n after 20 weeks


starting value: 6.5% active chlorine

33

1.5% SAS + 1% amine oxide

LAS

n Savinase 16L, c = 0.3%


n Lipolase 100L, c = 1.0%
c surfactant 3.0g/L, water hardness 179ppm CaCO3 (10d),
temperature 25C

Hostapur SAS

chemical properties

In modern detergent formulations the use of soil release polymers


(SRP) is gaining increasing importance. Soilrelease polymers
improve the detachment of oily and fatty soil from fabrics containing synthetic fibres, especially polyester and polyester blended
fabrics. They are now included in the top brands of most detergent
manufacturers.
However, it is known that the effectiveness of these polymers is
dependent substantially on the type of surfactants in the detergent.
The literature describes, how the soil release effect is generally
reduced in combination with anionic surfactants.56 However, these
studies are restricted to the major anionic surfactants in detergents,
e.g. linear alkyl benzene sulphonate.

Fig. 17 shows that in combination with Hostapur SAS, unlike


combinations with linear alkyl benzene sulphonate or alkyl
sulphate, a significant improvement in the soil release effect is
achieved.
As is evident from fig. 18, the builder system as well as the
surfactant influences the performance of soil release polymers.
The soil release polymer reaches its greatest effectiveness with
the combination of Hostapur SAS plus the zeolite/soda system.
The combination of the polymer with Hostapur SAS plus sodium
tripolyphosphate (STPP) is more effective than the combination
with linear alkyl benzenesulphonate plus STPP.

The soil release effect of a commercial soil release polymer in


combination with Hostapur SAS was therefore investigated in
comparison with combinations with linear alkyl benzene sulphonate (LAS) or alkyl sulphate (AS) in the well-known dirty motor
oil test.

Figure 17: Improvement in the soil release effect by Hostapur SAS

Figure 18: Influence of the builder system on the performance


of soil release polymers

40

35

remission R [%]

remission R [%]

30
30

20

10

25
20
15
10
5
0

0
SRP

LAS

n 0.06 g/L SRP


n 1.0 g/L surfactant without SRP
n 1.0 g/L surfactant + 0.06 g/L SRP

34

AS

SAS

LAS
+ 2.0 g NTPP

LAS
+ 1.5 g zeolite
+ 0.7 g soda

SAS
+ 2.0 g NTPP

n 0.05 g/L surfactant + builder without SRP


n 1.0 g/L surfactant + builder + 0.06 g/L SRP

hostapur SAS

SAS
+ 1.5 g zeolite
+ 0.7 g soda

Hostapur SAS shows less tendency than other surfactants to form


liquid crystalline phases or gels. Hostapur SAS is therefore very
suitable for concentrates and liquid formulations.

Solubility in water

The very good solubility of the Hostapur SAS grades in water is


illustrated in fig. 19. As expected, the dissolving rate increases
sharply as the temperature of the water rises.

Low-temperature properties

Hostapur SAS has good low-temperature properties, especially


in high application concentrations. This applies particularly in
comparison with linear alkylbenzene sulphonate. Fig. 20 shows
in graph form the low-temperature clear and cloud points of the
individual Hostapur SAS (SAS)/alkyl ether sulphate (LES) mixtures.

Figure 19:

Solubility of the Hostapur SAS grades in distilled water

concentration c [g/100g]

80
70

The low-temperature cloud points of Hostapur SAS as a function


of the concentration are shown in fig. 21.

60
50
40
30
20
10
0
-10

10

20

30

40

temperature [C]
n SAS 30

n SAS 60

n SAS 93

Figure 20: Low-temperature cloud and clear points of 30%


Hostapur SAS/alkyl ether sulphate mixtures

Figure 21: Low-temperature properties of Hostapur SAS as a function

of the concentration
35

temperature [C]

35

temperature [C]

30
25
20
15
10

25
20
15
10
5

-5

-5

-10

-10
10

15

20
concentration c [%]

n SAS

35

30

n LAS

25

30

10

15

20
concentration c [%]

n SAS:AES 4:1

n LAS:AES 4:1

25

30

Hostapur SAS

Toxicological
and environmental
properties

36

hostapur SAS

A modern surfactant must not present


any risk to humans, animals,
plants and the environment during
manufacture, storage, transport,
processing, use and in the waste water.
As the following data show, Hostapur SAS is an environmentally
friendly surfactant with very good biodegradability, good
ecotoxicological values and good dermatological and toxicological
compatibility that has been successful for decades. It is safe to
use and poses no risk to the environment.
Detailed reports on the toxicology and environmental properties of
secondary alkane sulphonate are available in the literature. 57 74

37

Hostapur SAS

toxicological
profile

To confirm the favorable toxicological profile of Hostapur SAS,


extensive toxico-logical and dermatological investigations were carried
out over many years. The most important test results are given below:

Chronic toxicity

LD50 (rat) = appr. 5000 mg/kg (60%)


LD50 (mouse) = appr. 2900 mg/kg (60%)
LD50 (mouse) = appr. 1900 mg/kg (93%)

Hostapur SAS (60%) was tested for chronic toxicity and/or carcinogenicity in two longterm studies on rats and mice. No toxicologically significant effects were observed after oral administration to
rats of up to 2% in the feed over a period of two years. In addition,
no signs of toxicity, either macroscopic or microscopic, were observed afterdermal application (three times per week for 80 weeks)
to mice.

Skin and mucous membrane irritation

Toxicokinetics

Animal studies conducted in accordance with OECD guideline 405


lead to the assumption that Hostapur SAS as well as other basic
surfactants, e.g. LAS, irritates both the skin and the eyes. Below a
threshold concentration (of 15% active detergent), however, no significant irritant effects are observed. Furthermore, well-documented human studies showed no indications of skin irritation caused by
diluted Hostapur SAS solutions.

The toxicokinetic properties of radioactively labelled Hostapur SAS


were investigated on rats. After oral adminis-tration, a dose-independent two-phase elimination with half-lives of 11 and 65 hours
was observed. Over 90% of the dose administered was excreted
within 24 hours.

Acute oral toxicity

Comparable toxicokinetic properties were also observed after dermal application to rats.

Sensitization

Hostapur SAS (60%) was tested in the Magnusson and Kligman


maximization test and proved not to be skin-sensitizing.
Mutagenicity

Hostapur SAS was tested in the AmesTest (S9) with Salmonella


typhimurium and for chromosome mutations in the micronucleus
test in vivo. In both test systems Hostapur SAS was not mutagenic.
Reproduction toxicity

Hostapur SAS (60%) was tested in a two-generation trial for possible reproduction toxicity properties. Up to a dose of 10,000ppm in
the feed, no maternotoxic, embryotoxic and/or teratogenic effects
of any kind were observed.

Conclusion: Hostapur SAS

is not sensitizing to skin.


is not mutagenic and/or genotoxic.
presents no risk in respect of reproduction toxicity.
exhibited no systemic toxicity in two long-term studies and
was not carcinogenic.
shows no signs of bio-accumulative potential and is eliminated
very rapidly.

In accordance with the CESIO classification Hostapur SAS


with an active detergent content of over 15% must be labelled as
irritant (Xi) whereas up to an active detergent content of 15%,
Hostapur SAS does not require a hazard warning label.
For detailed information see Safety data sheet.
Hostapur SAS does not present a health risk
under conditions of use.

38

hostapur SAS

Hostapur SAS
Ecology

Biodegradability

Secondary alkane sulphonates are readily and rapidly biodegradable. The primary degradability is considerably in excess of 90%.
In the OECD Confirmatory Test (sewage sludge simulation test)
the rate of degradation is 99% (decrease in MBAS). In the modified
OECD Screening Test (OECD 301 E), a test for total degradability,
SAS has a DOC removal of 95%. The Ten-days-window criterion
is thus met, i.e. SAS is readily biodegradable.
Compared with linear alkyl benzene sulphonates (LAS), secondary
alkane sulphonates (SAS) are more rapidly biodegradable. This applies especially at low temperatures. The degradation properties of
secondary alkane sulphonates are shown on page 51.
In the Coupled Units Test (OECD 303 A, sewage treatment plant
simulation test), the biodegradation/elimination is 96% +/-3%.
In a modified Coupled Units Test, in which the sewage treatment
plant simulation was better matched to the conditions in a modern
municipal sewage treatment plant, 99% +/- 1% secondary alkane
sulphonates were degraded/eliminated (DOC decrease).

39

Hostapur SAS
Ecology

Aquatic toxicity

Simplified risk assessment

Current data on the acute and chronic ecotoxicity and water


biocenosis toxicity are given in tabular form in Technical data:

A simplified qualitative risk assessment for Hostapur SAS shows


that there is a sufficiently large safety margin between exposure
concentration and effect concentration, the PEC/PNEC-ratio is
far below 1.

Possible toxic effects of surfactant as well as decomposition and


cleavage products of the secondary alkane sulphonate were
investigated in five pilot plants, in which the route taken by the
anionic surfactant from the consumer via the sewage treatment
plant to the surface water is simulated. Flora and fauna of the
-mesosaprobic zone were used as indicators of the effect on living
organisms. In addition, the embryolarval test was used to determine
the toxic substances in the water.
The results can be summarized as follows: High COD, BOD and
MBAS degradation rates of 90% were measured.

The data used for the qualitative risk assessment are given in the
table in Technical data.

Conclusion:

Based on data risk assessment Hostapur SAS there is only slight


anaerobic degradability of secondary alkane sulphonates, like
surfactants with a C-S bond, has no adverse effect on the environmental properties on the basis of the available data.

A slightly toxic effect (toxic is defined as an adverse effect on


health, growth and reproduction) on the green algae species
Spirogyra as a typical representative of the -mesosaprobic zone
was observed at 40ppm secondary alkane sulphonate in the water.

Conclusion

The surfactant has no significant effect on golden orfes and zebra


fish. Surfactant residues and cleavage products have no significant
toxic effect on the development of Cichlasome nigrofasciatum
larvae into the fully grown organism.
Secondary alkane sulphonate has no significant toxic effect on
Planorbis corneus.
Secondary alkane sulphonate has no significant toxic effect on
Daphnia magna. On the basis of the EU labelling criteria in
accordance with the 12th harmonization of Directive 91/325/EEC
no environmental labelling is required for alkane sulphonates.

40

hostapur SAS

Hostapur SAS

Life cycle assessment

A balance sheet on the production of the most important surfactants


at present used in detergents in Europe was drawn up by the
European LCI Surfactant Study Group (CEFIC/ECOSOL)
and Franklin Associates Ltd. (Tenside Surfactants Detergents 32
(1995) 2, 84 ff.).
In particular the surfactants linear alkyl benzene sulphonate (LAS),
alkyl sulphate (AS), alkyl ether sulphate (AES), soap, secondary
alkane sulphonate (SAS), fatty alcohol ethoxylate (AE) and
alkyl polyglucoside (APG) were studied. These are obtained
from petrochemical and oleochemical intermediates. The balance
sheet is extremely comprehensive and includes the energy and
material requirements as well as the emissions into the environment and the production of waste, which are associated with all
stages of surfactant manufacture. In accordance with the principles
recommended by the SETAC, a Peer Review Panel has assessed
the study.
The study shows that each system has effects on the environment
through the consumption of many different raw material sources
such as oil, natural gas, oleochemical/agricultural products and
of minerals as starting materials as well as through energy production and transport. On the basis of the results, there is no clear
scientific justification for singling out one of the systems as having
a fundamental environmental advantage, either for the production
of individual surfactants or for the various raw material sources,
which range from petrochemical and oleochemical/agricultural
raw materials to minerals.
The raw material consumption and the emissions into the environment in the manufacture of secondary alkane sulphonate (SAS)
by sulphoxidation of n-paraffin can be summarized as follows:
734kg oil, 105kg sulphur (for SO2) 138kg salt (for NaOH), 36kg
oxygen (for sulphoxidation) are required for the production of
1000kg SAS.

41

The total raw material consumption including the required energy


is 797kg oil, 154kg natural gas, 180kg coal.
Of the total energy consumption of 51.9 GJ, process energy accounts
for 36%; of the process energy 48% is apportioned to the SAS
stage. 68% of the total energy requirement is covered by oil.
The production of 1,000kg SAS gives rise to 64.2kg solid waste,
of which 84% comes from the oil; the emissions into the environment amount to 38kg. They stem mainly from the production
and incineration of the oil.

Conclusion:

Hostapur SAS has a favourable energy balance sheet, especially


when compared with alkyl ether sulphates. Furthermore it has
good values in respect of the solid waste occurring in production.

Hostapur SAS
Processing

42

hostapur SAS

Hostapur SAS can be supplied


in the following forms
liquid

= Hostapur SAS 30

paste

= Hostapur SAS 60

pellets

= Hostapur SAS 93

fine granules = Hostapur SAS 93 G

The homogenous Hostapur SAS 30, which is a clear liquid at


room temperature, is easy to transport, convey and store.
Hostapur SAS 60, by contrast, is a paste that flows at +20C
but that separates out into two phases of different composition
if left to stand for a lengthy period of time. For this reason
Hostapur SAS 60 must be homogenized before use by stirring
and, if necessary, by heating. This measure is not necessary
if full drums are completelyprocessed.

43

Hostapur SAS

Transport and storage

Transport

Storage

The loading temperature ex works for delivery by road tanker is for

Containers made from the following materials have proved


successful for storing the Hostapur SAS grades:
fibre-glass-reinforced polyester resin, especially for storage
tanks with a capacity of 3070 m3,
steel containers with suitable hard rubber lining or with
tried and tested internal coatings, for example, epoxy resin
or phenol-formaldehyde resin,
stainless steel, for example, material no. 1.4541 (V2A)
or 1.4571 (V4A).

Hostapur SAS 30 5060C and for


Hostapur SAS 60 7090C.
Although Hostapur SAS 60 is still pumpable at room temperature
with the pumps mentioned in section Conveying/mixing, the
temperature during transport should not fall below 65C so as to
facilitate handling and conveying. The road tankers intended for
transporting Hostapur SAS 60 have standard R 3 connections or
conventional hose couplings.

The last-mentioned materials are also recommended for


pipelines.
An example of the installation of a storage tank is shown
diagrammatically in fig. 22.
Before storage tanks are installed, a guarantee of compatibility
with Hostapur SAS at the intended storage temperatures should
be obtained from the manufacturer in question.

44

hostapur SAS


Fig. 22: 60-t storage tank
for Hostapur SAS 60

floating
distribution
system

stainless steel
carbon steel rubber lined
fibre-glass reinforced polyester

stainless steel
carbon steel rubber lined
fibre-glass reinforced polyester

insulation
steam 2-5 bar
feed
hose

Heat Exchanger
condensate
Production

T > 65 C

Filter
sampling
Tank

Hostapur SAS 30 should be stored at temperatures above 20C,


because cloudiness may occur at lower temperatures. This
cloudiness has no effect on the quality of the product. Before use,
however, the product must be homogenized.
As already mentioned, Hostapur SAS 60 separates out in storage
into two phases, one containing more surfactant than the other.
In addition, sodium sulphate can separate out at fairly low
temperatures. It is therefore necessary to stir or pump round the
tank contents constantly and at the same time to maintain a storage
temperature of 6590C. If a circulating pump is used, entrainment
of air must be prevented by suitable design of the return pipe.
Our experts will gladly provide technical advice on planning and
installing storage tanks for Hostapur SAS grades.

45

Pump

Hostapur SAS 93 presents no problems in transport and processing.


When processing Hostapur SAS 93 G, fine dust formation caused
by abrasion can be expected. Hostapur SAS 93 and 93 G can be
kept almost indefinitely under normal conditions but, since they
are hygroscopic, must be kept away from contact with water and
atmospheric moisture.

Hostapur SAS

Conveying/mixing,
Dilution, Handling

Conveying/mixing

Dilution of Hostapur SAS 60 to 30% or less

The rheological properties of Hostapur SAS 30 and Hostapur SAS


60 that are important for conveying are shown in figs. 2325 below.
Hostapur SAS 30 and 60 can be conveyed by displacement pumps
such as
gear pumps, supplied by e.g. Hermetic,
79194 Gundelfingen, Germany
Mohno pumps, supplied by e.g. Netzsch,
84478 Waldkraiburg, Germany
helical blade pumps or twin-screw displacement pumps made
of stainless steel, supplied by e.g. Bornemann,
31676 Obernkirchen, Germany.

than 30% active detergent

For homogenization, current models of low-speed stirrers can


be used. It is important to eliminate eddying so as to prevent
entrainment of air = foam formation. The stirrer blade should
therefore rotate below the surface of the liquid. Good results
have been obtained with low-speed interference-multistageimpulse-counterflow stirrers (INTERMIG), supplied by Ekato,
79650 Schopfheim, Germany.

The storage of Hostapur SAS 60 can be simplified by adjusting the


product on delivery to 30% or less active detergent by diluting it
with water.
Any stirred vessel made of suitable material, see section Storage,
with low-speed stirrers can be used. The soft and preserved water
intended for dilution (hot water accelerates the dilution operation)
is run into the vessel and the Hostapur SAS 60 is added and dissolved with slow stirring (eddying should be avoided because
of foam development). The product can also be homogenized by
being pumped round.
Another possibility consists of running Hostapur SAS 60 into
the storage tank and at the same time slowly adding hot water.
The amount of water is governed by the efficiency of the pumps
and should be no more than one-fifth of the amount pumped r
ound per hour.
An example will illustrate this: Delivery of 20 t Hostapur SAS 60;
tank size 50 m3; pumping rate 5 m3/h; water added 1/5 of 5 m3 =
1 m3/h. In this case it takes about 20 hours to produce 40 t
Hostapur SAS 30 from 20 t Hostapur SAS 60.

Figure 23: Viscosity of Hostapur SAS 30 measured with a Brookfield


viscometer RVT , spindle 1, speed 20 min-1

Figure 24: Viscosity of Hostapur SAS 60 as a function of the shear rate,


measured in a HAAKE-Rotovisco RV 20

300

10000

viscosity [mPas]

viscosity [mPas]

5000
200

100

0
20

1000
500

200
100

30

40

50

temperature [C]

46

2000

60

10

15

70

20

25

30

shear rate D [s-1]


n 50C n 20C

hostapur SAS

35

40

45

50

Dissolving of Hostapur SAS 93

The solid Hostapur SAS 93 can be dissolved in water in any vessel


made of suitable material and equipped with a low speed stirrer.
The solution is produced by running soft water or condensate
(5060C) into the vessel and slowly stirring in Hostapur SAS 93.
Stirring is continued until the Hostapur SAS 93 has completely
dissolved. Experience shows that this takes about 1530 minutes.
If a preservative has not already been added to the water used for
dissolving the solid matter, the resulting diluted Hostapur SAS
solution must be protected against bacterial attack by the addition
of suitable preservatives.
Water, which is used for dissolving, is one of the most likely
sources of contamination. Hygienic condtions are an indispensable
prerequisite for achieving a good commercial product. This applies
to the ion exchange resins, storage tanks, valves and ventilation
ducts as well as to the pipelines. A high standard in plant hygiene
is always crucial to the manufacture of finished products containing a low and harmless level of bacteria. Additional preservation
ensures that the end product reaches the consumer in a perfect
condition.

Figure 25: Viscosity of Hostapur SAS 60 as a function of the temperature

viscosity [mPas]

at D=10 s-1, measured in a HAAKE-Rotovisco RV 20


8000

Handling

7000

Because of the strong wetting and degreasing action, appropriate


protective measures should be taken, particularly where lengthy
exposure is involved. Therefore protective gloves and safety goggles
should be worn when handling these raw materials.

6000
5000
4000
3000
2000
1000
0
20

30

40

50

temperature [C]

47

The choice of the most effective preservative or frequently also


of combinations of several preservatives is dependent on the composition of the formulations and often also on national legislation.
Consequently, no universally effective type of preservative can be
recommended here. Hostapur SAS is however fully compatible
with most of the preservatives used in detergents and cosmetic
cleaners. Experience shows that the bacteriostatic effect improves
with increasing content of Hostapur SAS and the corresponding
co-surfactants. This means that the amount of preservative can
usually be reduced. In extreme cases it is even possible to dispense
with preservatives altogether. Adjustment of the pH to a weakly
acid value can also bring an improvement in preservative action.
Whereas Hostapur SAS is stable in the acid pH range, the susceptibility of surfactants with ester groups to hydrolysis must be borne
in mind. Generally speaking, it is advisable to conduct storage tests
with compatibility studies and to test compatibility with the packaging.

60

70

Hostapur SAS

Technical Data
and Literature

48

hostapur SAS

Summary of the properties


of Hostapur SAS:
Good solubility

the low viscosity of more highly concentrated solutions thus permits:


easy manufacture of liquid detergents and cleaners
saving of packaging costs
reduction in the use of hydrotropes
Excellent electrolyte compatibility
Chemical stability over the entire pH range
Excellent stability in the presence of oxidizing agents,
for example, hypochlorite
Saving of enzymes
Good cleaning and degreasing properties
Good foaming power
Pale inherent colour
Good detergent action
Good skin compatibility
Rapid biodegradability

49

Hostapur SAS

Physical/chemical data

Guide product data


Feature

Hostapur SAS 30

Hostapur SAS 60

Hostapur SAS 93

Hostapur SAS 93 G

Appearance at 20C

clear faintly yellowish liquid

yellowish soft paste

yellowish waxy pellets

yellowish fine granules

Average molecular weight

328gmol-1

328gmol-1

328gmol-1

328gmol-1

Active detergent content

approx. 30%

approx. 60%

approx. 93%

approx. 93%

Sodium sulphate content

max. 2.1%

max. 4.2%

max. 6.5%

max. 7.0%

Paraffin content

max. 0.4%

max. 0.7%

max. 1.0%

max. 1.0%

pH 5% as is in water

7.08.5

7.08.5

about 7.08.5

about 7.08.5

Bulk density

about

Particle size (average fineness)

Density (gcm-3)

600gL-1

about 570gL-1
< 1mm (75%)

Calorific data

Temperature

Hostapur SAS 30

Hostapur SAS 60

20C

1.048

1.087

Specific heat

30C

1.042

1.081

40C

1.036

1.075

50C

1.031

1.068

60C

1.025

1.062

Thermal conductivity

70C

1.017

1.055

W m-1 K-1

0.47

0.28

80C

1.049

(kcal m-1 h-1 C-1)

(0.40)

(0.25)

50

Hostapur SAS 30

Hostapur SAS 60

kJ kg-1 K-1

3.56

2.76

(kcal kg-1 C-1)

(0.85)

(0.66)

hostapur SAS

Hostapur SAS

Ecological data

Biodegradability

% biodegradation

OECD Confirmatory Test

99

Mineralization (DOC)
SAS after 6 days (OECD Screening Test 301 E)

87

Radiolabelled experiments
SAS (U-14C) after 6 days

45

Laboratory tests at low temperatures in a trickling filter plant


SAS degradation at +1C air temperature (+8C in trickling filter)

85

Biodegradation in the OE CD Coupled Units Test (OE CD 303 A)

> 90

C-chain distribution

< C13 n-Paraffin

max. 1%

C13-C15-n-Paraffin

about 58%

C16-C17-n-Paraffin

about 39%

> C17 n-Paraffin

max. 2%

Monosulphonate*

about 90%

Disulphonate*

about 10%

* calculated on 100% active detergent

Registration status

Chemical name in accordance with IUPAC


INCI name: Sodium C14-17 sec-Alkyl Sulphonate
Registered in Japan (MITI)
Registered in Korea, USA, Canada, Switzerland, Australia
Labelling in accordance with 12th harmonization directive
91/325/EWG: no environmental hazard labelling required

51

Hostapur SAS

Ecological data

Aquatic Toxicity
Acute toxicity

Fish toxicity (golden orfe, 48 h, OECD 203)

LC0

7.1mg L-1

LC50

8.4mgL -1

LC100

9.9mgL -1

Guppy

LC50

3.6mgL -1

Trout

LC50

2.8mg 0L-1

Carp

LC50

2.8mgL -1

Daphnia toxicity (Daphnia magna, 24 h, OECD 202)

EC50

12.5mgL -1

Fish toxicity

Bacterial toxicity (sewage sludge)

> 1000mgL -1

Chronic toxicity

EC10

58 mgL -1

Chronic bacterial toxicity (Bringmann-Khn)

EC50

95.5 mgL -1

Chronic algal toxicity (OECD 201)

LOEC

3.0 mgL -1

Chronic Daphnia reproduction test (OECD 202)

NOEC

0.37mgL -1

Coupled Daphnia multigeneration test (toxicity of the discharge from the modified
OECD Confirmatory Test on three consecutive generations of Daphnia)

no toxic effect

Water biocenosis toxicity

LOEC

3.5 (MBAS)

NOEC

1.4 (MBAS)

Risk Assessment of Hostapur SAS


1. Effects (NOEC) 1)

Fish

1.2mgL-1

Daphnia

0.6mgL-1

Algae

6.1mgL-1

2. Exposure (D, NL)

STP intake2)

0.5mgL -1

STP discharge

2gL -1

STP removal

99.6%

River water

< 1gL -1

3. PEC/PNEC3)4)

Fish/river water

> 1200

Daphnia/river water

> 600

Algae/river water

> 6100
0.03

3. Safety factors
1)

NOE C: no observed effect concentration,

2)

STP : sewage treatment plant, PE C: predicted environment concentration 4) PNE C: predicted no effect concentration
3)

Sources: 1. BUA-Stoffbericht 206, S. Hirzel Verlag. 2. Internal SAS exposure data

52

hostapur SAS

Hostapur SAS

Analysis,
Further information,
literature
Analysis

Further information

For literature on the analysis of secondary alkane sulphonates see


Literature. 75 92

Safety Data Sheet


Guide Formulations
Detergent Raw Materials Product Range

Synthesis

20 Hauthal, H.G., in: Anionic Surfactants, Marcell Dekker, Inc. New York,

1 Asinger, F. and Saus, A.: Beitrag zur Sulfoxidation von Paraffinkohlenwasser-

Basel, Hong Kong, (1995), 143-220

stoffen in Gegenwart von Gammastrahlen bzw. von ultraviolettem Licht, Arbeit

21 Crass, G.: Tenside Surf. Det. 30, (1993), 408

der TH Aachen (Techn. Chemie & Petrochemie), (1968)

22 Turowski, A., Antwerpen, W. and Jrges, P.: Vortrag beim Sepawa-

2 Berthold, H. and Lipfert, G., in: Alkansulfonate (H. G. Hauthal, ed.), VEB

Kongress, Bad Drkheim, (1994)

Deutscher Verlag fr Grundstoffindustrie, Leipzig, (1985), 13-50

23 Tischer, H., Wedler, C., Knofe, E. and Haage, K.: 6. Internationale Tagung

3 Commichau, A.: Zur Kenntnis der Sulfoxidation von Paraffinkohlenwasserstof-

ber grenzflchenaktive Stoffe. Abh. Akad. Wiss. DDR, NI (D. Vollhardt, ed.),

fen und zur Sulfoxidation bzw. Sulfochlorierung von Fettsuren. Doktorarbeit der

Akademie-Verlag, Berlin, (1987), 583-587

Universitt Aachen, (1965)

24 Grey, S., in: Proceedings of the 3rd World Conference on Detergents: Global

4 Beermann, C.: ber die Sulfoxidation von Paraffinen und die verbesserte

Perspectives (A. Cahn, ed.), AOCS Press, Champaign, IL, (1994), 82-87.

biologische Abbaubarkeit der Alkansulfonate, Symposium ber n-Paraffine in

25 Hauthal, H. G., Seichter, E., Sowada, R. and Trautmann, P., in:

Manchester, (1966)

Alkansulfonate (H.G. Hauthal, ed.), VEB Deutscher, Verlag fr

5 Schneider, G.: Neue Waschrohstoffe auf petrochemischer Basis, SFW, 26

Grundstoffindustrie, Leipzig, (1985), 143-178.

(1969)

26 Hoffmann, H., Hohlfeld, G., Quack, J. M.: Untersuchungen ber das

6 Hoechst AG: Hostapur SAS: The raw material with a sure future, (1987)

Viskosittsverhalten von Waschmittelslurries unter besonderer Bercksichtigung

7 Platz, C. and Schimmelschmidt, K.: Pionierpatent: DRP 735 096, (1940)

des Einflusses der Tenside, SFW 8, (1978), 209-212

8 Ramloch, H. and Tuber, G.: Moderne Verfahren der Grochemie: Die Sulfoxi-

27 Trautmann, M. and Jrges, P.: Tenside Detergents 21, (1984), 57-61

dation, Chemie in unserer Zeit. 13, (1979), 157-162

28 Trautmann, M.: New test method for assessing the cleaning action of all

9 Boy, A. et al.: Paraffin-sulfonates process boasts new extraction step Chemical

purpose cleaners, Vortrag anlsslich des spanischen Detergentienkongresses in

Engineering, 13, Oct., (1975)

Barcelona, (1985)

10 Graf, R.: Justus Liebigs Ann. Chem. 578, (1952), 50

29 Quack, J. M. and Reng, A. K.: Sekundres Alkansulfonat: Eigenschaften und

11 Graf, R.: DR P J 74599, (1943)

Einsatzmglichkeiten in kosmetischen Prparaten, Fette-Seifen-Anstrichmittel

12 Saus, A. et al.: Substitutionsverhltnisse bei der Disulfoxidation von

78, (1976), 200-206

Paraffinkohlenwasserstoffen, Tenside Detergents 10, 3, (1973), 113-119

30 Kleber, R. M.: Tenside Surf. Det. 31, (1994), 358

13 Orthner, L.: Angewandte Chemie 62, (1950), 302


14 Hauthal, H. G.: Alkansulfonate VEB Deutscher Verlag fr Grundstoffindustrie,

Physical and chemical properties

Leipzig, (1985)

31 Hauthal, H. G.: In Anionic Surfactants, Marcell Dekker, Inc. New York, Basel,
Hong Kong, (1995), 143-220

Applications

32 Hauthal, H. G. and Kretzschmar, G., in: Alkansulfonate (H.G. Hauthal, ed.),

15 Antwerpen, W. and Trautmann, M.: Formulierung hochkonzentrierter fls-

VEB Deutscher Verlag fr Grundstoffindustrie, Leipzig, (1985), 83-111.

siger Wasch- und Reinigungsmittel, SFW, (1984), 235-40

33 Hauthal, H. G., Mhle, L., Pfestorf, R. and Quitzsch, K.: Lecture to the 2nd

16 Siegel, D. and Quack, J. M.: Lessives Liquides A Usage Menager, Vortrag

World Surfactant Congress, Sect. C2, Paris, (May 1988), 24-27

Spanischer Detergentienkongress, Barcelona, (1978)

34 Hauthal, H.G., Mhle, L., Pfestorf, R. and Quitzsch, K., in: 4. Internationale

17 Mller, M., Quack, J. M. and Vitores, L.: Entfettung und deren Bewertung,

Tagung ber grenzflchenaktive Stoffe, Abh. der Akad. der Wiss. DDR, NI

SFW, 18,19, 20, (1980)

(D. VoIlhardt, ed.), Akademie-Verlag, Berlin, (1987), 63-71.

18 Krings, Andree, H.: Anwendungstechnische Eigenschaften der wichtigsten

35 Mhle, L., Hauthal, H. G. and. Quitzsch, K.: Z. Physik. Chem. 264, (1983), 281

Tensidtypen, Waschmittelchemie Hthig Verlag, 55-73

36 Mhle, L., Opitz, S. and Ohlerich, U.: Tenside Surf. Detergents. 30, (1993),

19 Trautmann, M.: Tenside Detergents 18, (1981), 73-78

104-109

53

Hostapur SAS
literature

37 Ekwall, P. Mandell, L. and Fontell, K.: Mol. Cryst. Liquid Cryst. 8, (1969), 157

67 Ltzsch, K., Neufahrt, A and Tuber, G.: Tenside Det. 16, (1979), 155-155

38 Frumkin, A.: Z. Phys. Chem., Leipzig 116, (1925), 466

68 Neufahrt, A., Ltzsch, K. and Weimer, K.: Radiometric studies of the

39 Kunieda, H. and Arai, T.: Bull. Chem. Soc. Jpn. 57, (1984), 281

biodegradation of sec. alkane sulfonate in a sewage plant model, Inter. Deter.

40 L in, I. J. and Somasundaran, P. J.: Colloid Interf. Sci. 37, (1971), 731

Congress Barcelona, (1980)

41 Lunkenheimer K. and Miller, R.: Tenside Det. 16, (1979), 312

69 Satake, I. and Matuura, R.: Bull. Chem. Soc. Japan 36, (1963), 813-817

42 Lunkenheimer, K. and Kretzschmar, G.: Z. Physik. Chem. 256, (1975), 593

70 Schberl, P.: Tenside Surf. Det. 28, (1991), 6

43 Lunkenheimer, K., Miller, R. and Becht, J.: Colloid Polymer Sci. 260, (1982),

71 Scholz, N. and Mller, F. J.: Chemosphere 25, (1992), 563

1145

72 Scholz, N.: Tenside Surf. Det. 28, (1991), 277

44 Rosen, M. J. and Murphy, D. S. J.: Colloid Interf. Sci. 110, (1986), 224

73 Schwuger, M. J.: Chem.-Ing. Techn. 42, (1970), 433-438

45 Saito, M., Moroi, Y., and Matura, R. J.: Colloid Interf. Sci. 88, (1982), 578

74 Stalmans, M. and Berenbold, H. et al: European Life-Cycle Inventory for

46 Sowada, R. J.: Prakt. Chem. 323, (1981), 93

Detergent Surfactants Production, Tenside Surf. Det. 32, (1995), 84-109

47 Sowada, R. J.: Zur Berechnung des HLB-Wertes isomerer und substituierter


Alkansulfonate, Journal f. prakt. Chemie, 322, (1980), 723-729

Analysis

48 Sowada, R. J.: Prakt. Chem. 322, (1980), 590

75 Arens, M., Waldhoff, H. and Pfeiffer, H.: Fat Sci. Technol. 96, (1994), 107-112

49 Sowada, R. J.: Prakt. Chem. 322, (1980), 723

76 Berthold, H. and Janot, I., in: Alkansulfonate (H. G. Hauthal, ed.), VEB Deut-

50 Sowada, R. J.: Prakt. Chem. 323, (1981), 951

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51 Vold, M. J.: Colloid Interf. Sci. 90, (1982), 543-545

77 Berthold, H. and Lipfert, G., in: Alkansulfonate (H. G. Hauthal, ed.), VEB

52 Asinger, F., Ebeneder, F. and Richter, G.: ber den Einfluss von Disulfonaten

Deutscher Verlag fr Grundstoffindustrie, Leipzig, (1985), 28-32

auf die oberflchenaktiven und waschtechnischen Eigenschaften von Monosulfo-

78 Eppert, G. and Liebscher, G. J.: Chromatogr. 356, (1986), 372-378

naten, Journal fr prakt. Chemie, 4. Reihe, Band 2, (1955)

79 Eppert, G. and Liebscher, G. J.: Chromatogr. Sci. 29, (1991), 21-25

53 Asinger, F. and Freitag, G.: ber den Einfluss von Tetradekandisulfonaten auf

80 Field, J. A., Miller, D. J., Field, T. M., Hawthorne, S. B. and Giger, W.: Anal.

die oberflchenaktiven und waschtechnischen Eigenschaften von Tetradekanmo-

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81 Field, J. A., Field, T. M., Poiger, T. and Giger, W.: Environ. Sci. Technol. 28,

54 Sowada, R.: Zur Berechnung der mizellaren Aggregationszahl homologer und

(1994), 497-503

isomerer Alkansulfonate, Journal f. prakt. Chemie, Band 323, (1981), 951-956

82 Field, J. A., Field, T. M., Poiger, T., Siegrist, H. and Giger. W.: Wat. Res. 29,

55 Miller, D.: Emulgierwirkung als Splmitteltest, SFW-Journal 122, (1996),

(1995), 1301-1307

406-408

83 Hummel, D. O.: GIT Fachz. Lab. 38, (1994), 439-447

56 WF K Forschungsprojekt AiF.FV Nr. 10186, WFK-Forschungsinstitut fr

84 Kloster, G., Schoester, M. and Schwuger, M. J.: Journ. Com. Esp. Deterg. 24,

Reinigungstechnologie e.V., D-47798 Krefeld

(1993), 25-33
85 Klotz, H. and Spilker, R.: Tenside Surf. Det. 29, (1992), 13-15

Toxicological and environmental properties

86 Liebscher, G. and Eppert, G.: Chem. 19, (1979), 69

57 Anionic Surfactants: Biochemistry, Toxicology, Dermatology, 2nd ed., revised

87 Liebscher, G., Eppert, G., Oberender, H., Berthold, H. and Hauthal, H. G.:

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Tenside Surf. Det. 26, (1989), 195

Vol. 43, Marcel Dekker, New York, (1992)

88 Liebscher, G.: Lecture to the Merck Forum, 14. Sept. 1994.

58 Bennen, J. A., Ruckenstein, E. and Coll, J.: Interface Sci. 96, (1983), 469-487

89 Mahr, S. A., Wangsa, J. and Danielson, N. D.: Anal. Chem. 64, (1992), 583-589

59 Bercovici, R., Krmann, H.: Welttensidkongress Mnchen, (1984)

90 Schmitt, T. M., in: Analysis of Surfactants (M. J. Schick and F. M. Fowkes,

60 Berenbold, H. and Kosswig, K.: Tenside Surf. Det. 32, (1995), 152-156

eds.), Vol. 40 of Surfactant Science Series, Marcel Dekker, New York, (1992),

61 Brndel, S. and Dietzsch, K., in: Alkansulfonate (H. G. Hauthal, ed.), VEB

37-40

Deutscher Verlag fr Grundstoffindustrie, Leipzig, (1985)

91 Schoester, M., Kloster, G. and Fresenius, J.: Anal. Chem. 345, (1993), 767-772

62 Giesser, R.: Tenside Detergents 20, (1983), 25-527

92 Zhou, D. and Pietrzyk, D. J.: Anal. Chem. 64, (1992), 1003-1008

63 Gilbert, A. and Pettigrew, R.: Surfactants and the Environment, lnter. Journal of Cos. Science 6, (1984), 149-158
64 Gloxhuber, C.: Arch. Toxicol. 32, (1974), 245-270
65 Hrsak, D., Bosnjak, M. and Johanides, V.: Kinetics of linear Alkylbenzene
Sulfonate and sec. alkane sulfonate biodegradation, Tenside Detergents 18, (1981)
66 Krone, M. and Schneider, G.: Biochemische Abbaubarkeit von sek. Alkansulfonat unter Labor- und Praxisbedingungen, Fette-Seifen-Anstrichmittel 70,
(1968), 10
54

hostapur SAS

Hostapur SAS

Product range

type

Hostapur SAS 30

Hostapur SAS 60

INCI Name

Hostapur SAS 93

Hostapur SAS 93 G

Sodium C14-17 sec-Alkyl Sulphonate

CAS Numbers

97489-15-1; 85711-70-2; 85711-69-9; 68608-26-4; 68037-49-0

EINECS/ELINCS Numbers

307-055-2; 288-331; 288-330-3

Active Content [%]

29.230.8

59.061.0

91.594.5

90.593.5

Appearance

clear faintly yellowish liquid

yellowish soft paste

yellowish waxy pellets

yellowish fine granules

Sodium sulphate [%]

max. 2.1

max. 4.2

max. 6.5

max. 6.5

Paraffin [%]

max. 0.4

max. 0.7

max. 1.0

max. 1.0

Viscosity [nPas, 20C]

approx. 300

approx. 7500

Density [gcm-3]

approx. 1.048

approx. 1.087

approx. 600

550650

3.56

2.76

Thermal conductivitiy [Wm-1 K-1] 0.47

0.28

Bulk density

[gl-1]

Specific heat [kJkg-1 K]

55

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2013 Clariant International Ltd

05.2013

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