Language selection

Search

Patent 1046699 Summary

Third-party information liability

Some of the information on this Web page has been provided by external sources. The Government of Canada is not responsible for the accuracy, reliability or currency of the information supplied by external sources. Users wishing to rely upon this information should consult directly with the source of the information. Content provided by external sources is not subject to official languages, privacy and accessibility requirements.

Claims and Abstract availability

Any discrepancies in the text and image of the Claims and Abstract are due to differing posting times. Text of the Claims and Abstract are posted:

  • At the time the application is open to public inspection;
  • At the time of issue of the patent (grant).
(12) Patent: (11) CA 1046699
(21) Application Number: 1046699
(54) English Title: PROCESS FOR IMPROVING THE HEAT RESISTANCE OF EXPANDABLE POLYSTYRENE
(54) French Title: METHODE PERMETTANT D'AMELIORER LA RESISTANCE A LA CHALEUR DU POLYSTYRENE EXTENSIBLE
Status: Term Expired - Post Grant Beyond Limit
Bibliographic Data
Abstracts

English Abstract


Abstract of the Disclosure
The present invention relates to expandable polystyrene
beads showing a high resistance to heat at temperatures of
up to about 50°C. Said improved beads are obtained by in-
corporating into them 0.01 to 0.5% by weight of octafluorocy-
clobutane in addition to the usual hydrocarbon blowing agent.


Claims

Note: Claims are shown in the official language in which they were submitted.


THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE PROPERTY
OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. Beads showing a high resistance to heat at temperatures
of up to about 50°C, comprising a styrene polymer in admixture with
at least one blowing agent selected from the group of lower
aliphatic and cycloaliphatic hydrocarbons having 4 to 6 carbon
atoms, and from 0.01 to 0.5% by weight of octafluorocyclobutane,
the blowing agent being present in an amount of about S to 7.5%
by weight.
2. Beads as claimed in claim 1 in-which the styrene
polymer is a homopolymer of styrene or a copolymer thereof with
at least one member of the group of .alpha.-methylstyrene, acrylo-
nitrile, methacrylonitrile or a styrene alkylated in the nucleus.
3. Beads as claimed in claim 1, in which the octa-
fluorocyclobutane is present in an amount of from 0.1 to 0.3%
by weight.
4. Beads as claimed in claim 1, or claim 2 in
which the blowing agent is iso-pentane.
5. Beads as claimed in claim 1, claim 2 or claim 3 in
which a flame retarding agent is also present.
6. Beads as claimed in claim 1, claim 2 or claim 3 in
which pentabromophenylallyl ether is present as a flame retarding
agent in an amount of about 0.8% by weight.

7. A process for the preparation of beads of a styrene
polymer as claimed in claim 1, said beads showing a high resistance
to heat at temperatures of up to about 50°C in which
(a) styrene is homopolymerized or copolymerized with at least
one monomer selected from the group of .alpha.-methylstyrene,
acrylonitrile, methacrylonitrile or a styrene alkylated in
the nucleus, in an aqueous suspension in the presence of
at least one blowing agent and of from 0.01 to 0.5% by
weight of octafluorocyclobutane, or
(b) at least one blowing agent selected from the group of lower
aliphatic and cycloaliphatic hydrocarbons having 4 to 6
carbon atoms and 0.01 to 0.5% by weight of octafluoro-
cyclobutane are incorporated into a homopolymer of styrene
or a copolymer thereof with .alpha.-methylstyrene, acrylonitrile,
methacrylonitrile or a styrene alkylated in the nucleus.
8. A process as claimed in claim 7 in which the process
is carried out according to (a) and the polymer or copolymer is
formed in the presence of a free radical peroxide initiator and
a suspending agent and at a temperature of from 90 to 130°C.
9. A process as claimed in claim 7 in which the process
is carried out according to (b) and the beads of styrene polymer
are dispersed in water at a temperature of from 100 to 120°C
using a dispersing agent and the blowing agent and octafluoro-
cyclobutane are added thereto.

Description

Note: Descriptions are shown in the official language in which they were submitted.


HOE 74~E_100
~0~i99
The quality of a foamed polystyrene substantially depends
on the cellular structure and the density of the foamed shaped
article. A homogeneous cellular structure in the whole foamed
bloc or shaped article is desired. In the case of foamed
plastics obtained from polystyrene beads containing a blowing
agent the total cellular structure depends on the indi~idual
cellular structure of the prefoamed polystyrene beads and on
their optimum welding in the final foaming process. The
thermal treatment of the unfoamed polystyrene beads containing
a blowing agent is substantial for the quality of their cellu-
lar structure, the blowing agent and the content of blowing
agent being the same.
At the convention date of this application no expandable
polystyrene containing a blowing agent and any known nucle-
ating agent was known, which may be foamed after haYingbeen exposed to a temp=rature of from 40 to 50 C for one or
several hours prior to the prefoaming or foaming process to
give products having a density of about 14 g/l and a homoge-
neous fine cellular structure . The observations made hith-
erto confirm that the cellular structure more and more coar-
sens during s*orage at varying elevated temperature depending
on the time and the temperature, i.e. there are formed less,
but larger cellules at the expense of the small ones. The
- influence of heat especially acts on styrene polymers con-
taining a blowing agent and halides for preparing self-ex-
tinguishing foamed plastics. Some improvement may be obtained
by substituting n-pentane by isopentane as blowing ~gent, but
the fine cellular structure is also destroyed by storage at
29 a temperature of 50C for one hour.
. ~ .
:
. . . - ~ .
,':~

~ O
1()~6~;9g
It was known that 1-chloro-1,2,2,3$3,4,4-heptafluoro-
cyclobutane ~nd 1,2-dichloro-1,2,393,4,4-hexafluorocyclobutane
may be used as blowing agent for polystyrene in an amount of
>10% by weight, for example from German Auslegeschrift No.
1,241,976.
It has now been found that beads of a styrene polymer
containing a blowing agent, which comprise from 0.01 to 0.5
by weight, preferably of from Oo1 to 0.3~ by wei~ht of octa-
- fluorocyclobutane, show a high heat resistance at temperatures
of up to about 50 C and yield foams of a homogeneous fine
cellular structure when foaming them after exposure to heat.
A process has moreove~ been found for preparing beads of
a styrene polymer containing a blowing agent and ha~ing a
high heat resistance at temperatures of up to a~out 5V C by
- 15 homo- or copolymerization of monomeric styrene in aqueous
-- suspension in the presence of at leastone blowing agant or
by incorporating the blowing agent or a mixture of t~Jo or
se~eral blowing agents into the styrene polymer, which com-
prises adding to the blowing agent(s) from 0.01 to 0.5% by
. 20 weight, preferably from 0.1 to 0.3% by weight of octafluoro~
cyclobutane.
Among the styrene polymers suitable for ma~ing the beads
according to the invention there may be mentioned homopoly-
styrene or copolymers of styrene with ~methylstyrene, a
styrene alkylated in the nucleus, acrylonitrile or methacry- ~-
lonitrile
The polymerization of mIl~eriC styrene in aqueous suspe~-
sion initiated by free radicals ~xm ~ro~desis carried out ~cor-
29 ding to the Btate of the art, by using as suspending auxili-
~ ,. ,....... , . ~ . :
-~ ' -' ' . ' ' , .~ ; , -
, ' ' '.:, ' ,, :

HOE ~4/F 100
~1)4~i99
aries for exampls polyvinylalcohol, tricalcium phosphate
or polyvinylpyrrolidone. Examples of peroxides used are-di-
benzoylperoxide, tertiary butylperoctanoate, tertiary butyl-
perben~oate. The polymerization reaction is carried out in
the presence of the blowing agent at temperatures of from
90 to 130C.
Octafluorocyclobutane is suitably added togetherwith the
blowing agent, ad~antageously by dissolving the former in
the latter.
The polymerization is followed by the usual working up
such as cooling, centrifuging, drying and sieving.
Octafluorocyclobutane may also be added advantageously
in the impregnation process of sieved beads of polystyrene
in admixture with the blowing agent.
The preferred impregnation process is carried out at
temperatures of from 100 to 120 C with beads of polystyrene
suspended in water by means of dispersing agents such as
polyvinyl alcohol etc.. ~he impregnation of polystyrene with
the blowing agent/octafluorocyclobutane mixture may also be
effected in a suitable extruder according to known process~
es.
The blowing agents to be used are the usual lower ali-
phatic and cycloaliphatic hydrocarbons having from 4 to 6
carbon atoms, preferably the isomeric pentanes, especially
isopentane, in an amount of from about 5 to about 7.5% by
weight.
The invention is of great technical importance, especi-
ally for manufacturing plants in southern countries, especi-
29 ally for equatorial regions, but also for Europe. In these
,. - : : , : , :
:: . :: . ~ - :
. . . . . . . . .
- . . : . . , :. . . :
~ ' " ' : , ' ' '':' '

1046699
regions a heating of the expandable polystyrene to tempera~
tures of up to 50 C, for example in the storage or during
transportation may quite naturally occur in periods of hot
weather.
The following examples illustrate the inve~tion.
E X A M P L E S-
.
The examples manifest the technical progress obtained by
the invention at an extreme product temperature of 50 C.
The polymerization of styrene suspended in water in a
weight ratio of 1:1 was carried out for 8 hours at 90 C with
0.3~ by weight of dibenzoylperoxide and 0.15% by weight of
tertiary butylperbenzoate, both calculated on the monorneric
styrene. The dispersion was either effected with 0.3% by
weight of polyvinylpyrrolidone (PVP) or with 0.4% by weight
f tricalcium phosphate (TCP), both calculated on the monomerio
styrene. Aft~r the addition of 7.5~ by weight of blowing agent,
calculated on styrene, in admixture with the quantity of oc~a~
fluorocyclobutane, calculated on styrene)which is indicated
in the table, the reaction mixture was polymerized for 3
hours at 120 C, oooled to room temperature and separated
from the liquor by centrifuging while washing. The dried pro
ducts hav~ng aparticle diameter of from 800 to 1,600/u were
all prefoamed in the same manner with steam at a pressure
of 0.2 atmosphere gauge, stored at room temperature for 12
hours and welded at a pressure of about 0.3 atmosphere gauge
with steam in a mold of 5 cm X 10 cm X 10 cm (final foaming).
The foamed blocs stored for 1 day were cut into strips
having a ~ickness of 1 mm with a rotating knife and compared
29 qualitatively with a series oI` 10 structural standards. ~he
'
- 5 -
.. , . . , , . . . . , _ _ .. , _
. : . ~ . .
: -:

HOE 74/~ 100
10~99
values found are indicated in the following table in the co-
lumns he~ded "foam structure". Figures 1 to 6 show a sel.ection
of the structural standards in a 25-fold magnification:
figure l... standard 2
figure 2... standard 3
figure 3... st~ndard 5
~igure 4... stand~rd 6
figure 5... standard 7
figure 6... standard lO
The blowing agents used were n-C5=n-pentane having a maxi-
mum content of iso-pentane of about 25~7 and i-C5=iso-pen-
tane having a maximum content of n-pentane of 15~.
~n the examples 4, 5 and 8 to 15 an addi.tional flame-proo-
fing was performed by means of 0.8% by weight o~ pentabromo-
phenylallyl ether as flame retarding agent being added to the
polymerization mixture.
The reduced specific viscosity (RSV) of the polystyrene
was determined on solutions of 1 g of polystyrene in 100 ml
o~ toluene at 25C.
The results are given in the following table.
Example 3, 4 and 5 are comparative examples according to
the state of the art.
.
.
-,
.
. . ~
- . , .: .
::~ . . . : .. :
.

HOE 74/F` (35~9
~, 104~699
g
~,
O ~ h O ~ ~t ~~ O o~ ~ ~ cs~ c~ t~l h
tO ~ ~ W :~
td tJ td -O
~q 10
~:-- \o ~ ~ t~ t~ t.~ t.~ t~ tU tU u~ o h
A .. ~ ~d
~ o ~ r~ o o o ~ t~ t~ t~ t~
h ~ _ ~c ~ ~ 1::
~ U~ ~ tU 00 0 0 F~ t~ ~U tr~ t~ t~ tu t~ ~ ~
C) . td O
) t.~ N ~ t~ ~ t~ ~I tr~ l t~ ~ hr
U~ ~ _ *
~; tu o c~l t~u ~o ~ o ~ t~ t~`~
.
t~t~ t~t~tt~lt~t~t~-t~ a
_ tU t~Y ~ ::~ t~ ~ t.~l tU ~`1 N ~ t~ -- c\~ ~ O .~
. _ ` '''' I~ .
tu ~ ~ ~ o tU ~o t~ tu t~ tJ~ ca O o~
t 1~ t~ tJ~ 0~ 0~ t~ tJ~ 0~ t5~ 0~ t~ CO t~ tX~ tD
~1 O O O O O O O O O O O O O t; O ~ h
~1 ~ .. _. ' ' . !d
td h~t~t ~0 00 ~ ~O tJ~ ~ tS~ O 11~ 00 cr~ O tU S
- -~ tD bD-- O O -- -- ~ O O O ~ l t~U t~ 0
u 6 '~ -
rl O ~ ~ O O O O O O O O O O O O O O O :~
o ~. _I h
.~, ~ ~ .. ~ o o
a ~ , O~ t~ ~ t~0 ~ _ ~ O ~ ~ ~ ~ ~ h O~
t~ ~ ~o ~ ~ ~O \O ~ ~o ~o ~ ~o ~o
a ~ O __ n~ h td
h u~ u~ ~ ~ ~ u~ ~ u~ ~ u~ ~ ~ u~ ~ u- ~ ~;
C~ V C~ V V t~ V C~ V ~ ~ C) V O ~
O ~ I I II I 1- 1 1 1 1 1 1 1 1 i O ~I tD
I O, ... _ rl td u~
_I O tD ,qIt~ ~ o O O ~l t~ t'~ tU , O O u~ t.~l
h ~ qD. . ,~ . . . . . . . . . . td
t O t~ h- O O ~ ~ O O O O O O O O 0 O O
0 0 ~ ~ O
. ... __ . .
~31 tD bD ~: ~ ~4 P~ P~ ~ O
. p, ~ tD O V V ~ ,~ t~ tO U V 'O ~ ~ ~ ~
t ~ tD ~ P< ~ Pt O
_ ..... . _ h
x ~ _ tu t~ o ~ a~ t~ o t~ t~
., ~F~l ~ ~ 'C
, ~ ,
-- 7 --
.~. . . , - . - .. . . - , , ` . ,

Representative Drawing

Sorry, the representative drawing for patent document number 1046699 was not found.

Administrative Status

2024-08-01:As part of the Next Generation Patents (NGP) transition, the Canadian Patents Database (CPD) now contains a more detailed Event History, which replicates the Event Log of our new back-office solution.

Please note that "Inactive:" events refers to events no longer in use in our new back-office solution.

For a clearer understanding of the status of the application/patent presented on this page, the site Disclaimer , as well as the definitions for Patent , Event History , Maintenance Fee  and Payment History  should be consulted.

Event History

Description Date
Inactive: IPC from MCD 2006-03-11
Inactive: IPC from MCD 2006-03-11
Inactive: Expired (old Act Patent) latest possible expiry date 1996-01-16
Grant by Issuance 1979-01-16

Abandonment History

There is no abandonment history.

Owners on Record

Note: Records showing the ownership history in alphabetical order.

Current Owners on Record
HOECHST AKTIENGESELLSCHAFT
Past Owners on Record
None
Past Owners that do not appear in the "Owners on Record" listing will appear in other documentation within the application.
Documents

To view selected files, please enter reCAPTCHA code :



To view images, click a link in the Document Description column (Temporarily unavailable). To download the documents, select one or more checkboxes in the first column and then click the "Download Selected in PDF format (Zip Archive)" or the "Download Selected as Single PDF" button.

List of published and non-published patent-specific documents on the CPD .

If you have any difficulty accessing content, you can call the Client Service Centre at 1-866-997-1936 or send them an e-mail at CIPO Client Service Centre.


Document
Description 
Date
(yyyy-mm-dd) 
Number of pages   Size of Image (KB) 
Cover Page 1994-04-12 1 19
Abstract 1994-04-12 1 13
Drawings 1994-04-12 2 144
Claims 1994-04-12 2 65
Descriptions 1994-04-12 6 227