JP2002540249A5 - - Google Patents

Download PDF

Info

Publication number
JP2002540249A5
JP2002540249A5 JP2000606699A JP2000606699A JP2002540249A5 JP 2002540249 A5 JP2002540249 A5 JP 2002540249A5 JP 2000606699 A JP2000606699 A JP 2000606699A JP 2000606699 A JP2000606699 A JP 2000606699A JP 2002540249 A5 JP2002540249 A5 JP 2002540249A5
Authority
JP
Japan
Prior art keywords
weight
melamine
melem
composition
extruder
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2000606699A
Other languages
Japanese (ja)
Other versions
JP2002540249A (en
JP4303426B2 (en
Filing date
Publication date
Priority claimed from NL1011631A external-priority patent/NL1011631C2/en
Application filed filed Critical
Priority claimed from PCT/NL2000/000123 external-priority patent/WO2000056840A1/en
Publication of JP2002540249A publication Critical patent/JP2002540249A/en
Publication of JP2002540249A5 publication Critical patent/JP2002540249A5/ja
Application granted granted Critical
Publication of JP4303426B2 publication Critical patent/JP4303426B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【特許請求の範囲】
【請求項1】 10〜90重量%のメレム、
0.01〜30重量%のメラム、
0.01〜15重量%のメラミン、
0.1〜65重量%の、メラミンおよび/またはメレムのより高次の縮合生成物
を含み、揮発性物質含量が3重量%未満であり、ここで個々の成分の合計が100重量%である難燃性組成物。
【請求項2】 0.1秒より長い間、350〜800℃の温度で1KPa〜50MPaの圧力でメラミン含有出発物質を加熱することにより、10〜90重量%のメレム、0.01〜30重量%のメラム、0.01〜15重量%のメラミン、0.1〜65重量%の、メラミンおよび/またはメレムのより高次の縮合生成物を含み、揮発性物質含量が3重量%未満であり、ここで個々の成分の合計が100重量%である難燃性組成物を製造することを特徴とする、難燃性組成物の製造法。
【請求項】 下記成分:
a.65〜95重量%のポリマー含有組成物、
b.5〜35重量%の請求項1記載の難燃性組成物
を含む難燃性ポリマー組成物。
[Claims]
1-10% by weight of melem,
0.01-30% by weight of melam,
0.01 to 15% by weight of melamine,
From 0.1 to 65% by weight of higher condensation products of melamine and / or melem with a volatiles content of less than 3% by weight, wherein the sum of the individual components is 100% by weight Flame retardant composition.
2. Heating the melamine-containing starting material at a temperature of 350 to 800 ° C. and a pressure of 1 KPa to 50 MPa for more than 0.1 second to produce 10 to 90% by weight of melem, 0.01 to 30% by weight. % Melam, 0.01 to 15% by weight melamine, 0.1 to 65% by weight of higher condensation products of melamine and / or melem with a volatiles content of less than 3% by weight A method for producing a flame-retardant composition, comprising producing a flame-retardant composition in which the total of individual components is 100% by weight.
3. The following components:
a. 65-95% by weight of a polymer-containing composition,
b. A flame-retardant polymer composition comprising from 5 to 35% by weight of the flame-retardant composition of claim 1.

実施例13
米国特許第4565867号に従う方法で得られた、98.0%のメラミン、0.81%の尿素、0.03%のCO2、0.05%のアンメリン関連不純物(アンメリン、アンメリド、シアヌル酸およびウリドメラミンなど)および0.07%の有機固体(メレム、メラム、および酸素を含まない他の化合物)の混合物を、8kg/時の速度で、同時回転2軸スクリュ押出機(Werder& Pfleiderer, タイプZSK 30/33)に投入した。シリンダー温度は450℃にセットされており、スクリュ速度は40rpmにセットされていた。押出機に投入された成分の滞在時間は110秒であった。押出機を出る固体混合物は、白色〜淡いベージュ色であり、次の組成を有していた。すなわち、7重量%のメラミン、2重量%のメラム、76重量%のメレムおよび14重量%のメラミンおよび/またはメレムのより高次の縮合生成物、および約1重量%の未確認残留画分である。揮発性物質の含量は0.2重量%である。難燃性組成物の組成は、高圧液体クロマトグラフィー(HPLC)によって決定された。
Example 13
Obtained by the method according to U.S. Pat. No. 4,565,867, 98.0% of melamine 0.81% urea, 0.03% CO 2, 0.05% of the ammeline-related impurities (ammeline, ammelide, cyanuric acid and A mixture of uridomelamine and 0.07% of an organic solid (melem, melam and other compounds free of oxygen) is fed at a rate of 8 kg / h to a co-rotating twin screw extruder (Werder & Pfleiderer, type ZSK 30). / 33). The cylinder temperature was set at 450 ° C. and the screw speed was set at 40 rpm. The residence time of the components charged into the extruder was 110 seconds. The solid mixture exiting the extruder was white to light beige and had the following composition: 7% by weight of melamine, 2% by weight of melam, 76% by weight of melem and 14% by weight of higher order condensation products of melamine and / or melem, and about 1% by weight of the unidentified residual fraction. . The content of volatile substances is 0.2% by weight. The composition of the flame retardant composition was determined by high pressure liquid chromatography (HPLC).

実施例15
米国特許第3210352号に従う方法で得られた99.92%の純度を有するメラミンを、8kg/時の速度で、同時回転2軸スクリュ押出機(Werder &Pfleiderer製, タイプZSK 30/33)に投入した。シリンダー温度は450℃にセットされており、スクリュ速度は40rpmにセットされていた。押出機に投入された成分の滞在時間は110秒であった。押出機を出る固体混合物は、白色〜淡いベージュ色であり、次の組成を有していた。すなわち、6重量%のメラミン、1重量%のメラム、77重量%のメレムおよび16重量%のメラミンおよび/またはメレムのより高次の縮合生成物である。揮発性物質の含量は0.3重量%である。難燃性組成物の組成は、高圧液体クロマトグラフィー(HPLC)によって決定された。
Example 15
Melamine having a purity of 99.92%, obtained by a method according to US Pat. No. 3,210,352, was introduced at a rate of 8 kg / h into a co-rotating twin screw extruder (Werder & Pfleiderer, type ZSK 30/33). . The cylinder temperature was set at 450 ° C. and the screw speed was set at 40 rpm. The residence time of the components charged into the extruder was 110 seconds. The solid mixture exiting the extruder was white to light beige and had the following composition: 6% by weight of melamine, 1% by weight of melam, 77% by weight of melem and 16% by weight of melamine and / or higher condensation products of melem. The content of volatile substances is 0.3% by weight. The composition of the flame retardant composition was determined by high pressure liquid chromatography (HPLC).

実施例17
米国特許第3210352号に記載の方法に従って、冷却後でかつ結晶化の前に得られた、98.7%のメラミン、1.0%の尿素、0.06%のCO2、0.1%のアンメリン関連化合物(アンメリン、アンメリドおよびシアヌル酸など)および0.12%の有機固体(メレム、メラム、および他の化合物)および0.02%(200ppm)の残留無機触媒の混合物を、8kg/時の速度で、同時回転2軸スクリュ押出機(Werder& Pfleiderer, タイプZSK 30/33)に投入した。シリンダー温度は450℃にセットされており、スクリュ速度は40rpmにセットされていた。押出機に投入された成分の滞在時間は110秒であった。押出機を出る固体混合物は、白色〜淡いベージュ色であり、次の組成を有していた。すなわち、6重量%のメラミン、1重量%のメラム、74重量%のメレムおよび20重量%のメラミンおよび/またはメレムのより高次の縮合生成物である。揮発性物質の含量は0.3重量%である。難燃性組成物の組成は、高圧液体クロマトグラフィー(HPLC)によって決定された。
Example 17
98.7% melamine, 1.0% urea, 0.06% CO 2 , 0.1% obtained after cooling and before crystallization, according to the method described in US Pat. No. 3,210,352. Of an ammeline-related compound (such as ammeline, ammelide and cyanuric acid) and 0.12% of an organic solid (melem, melam and other compounds) and 0.02% (200 ppm) of a residual inorganic catalyst at a rate of 8 kg / hour. At the same speed, and fed into a co-rotating twin screw extruder (Werder & Pfleiderer, type ZSK 30/33). The cylinder temperature was set at 450 ° C. and the screw speed was set at 40 rpm. The residence time of the components charged into the extruder was 110 seconds. The solid mixture exiting the extruder was white to light beige and had the following composition: 6% by weight of melamine, 1% by weight of melam, 74% by weight of melem and 20% by weight of melamine and / or higher condensation products of melem. The content of volatile substances is 0.3% by weight. The composition of the flame retardant composition was determined by high pressure liquid chromatography (HPLC).

JP2000606699A 1999-03-22 2000-02-28 Flame retardant composition and process for producing the same Expired - Fee Related JP4303426B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
NL1011631 1999-03-22
NL1011631A NL1011631C2 (en) 1999-03-22 1999-03-22 Flame-retardant composition and method for its preparation.
PCT/NL2000/000123 WO2000056840A1 (en) 1999-03-22 2000-02-28 Flame-retarding composition and process for the preparation thereof

Publications (3)

Publication Number Publication Date
JP2002540249A JP2002540249A (en) 2002-11-26
JP2002540249A5 true JP2002540249A5 (en) 2007-03-29
JP4303426B2 JP4303426B2 (en) 2009-07-29

Family

ID=19768889

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000606699A Expired - Fee Related JP4303426B2 (en) 1999-03-22 2000-02-28 Flame retardant composition and process for producing the same

Country Status (11)

Country Link
JP (1) JP4303426B2 (en)
KR (1) KR100632555B1 (en)
CN (1) CN1192079C (en)
AT (1) ATE229062T1 (en)
AU (1) AU768261B2 (en)
BR (1) BR0009207A (en)
CA (1) CA2365173A1 (en)
DE (1) DE60000923T2 (en)
ES (1) ES2186632T3 (en)
NL (1) NL1011631C2 (en)
RU (1) RU2225876C2 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004076176A1 (en) * 2003-02-24 2004-09-10 E.I. Dupont De Nemours And Company Flame retardant surface coverings
US7758964B2 (en) * 2006-02-10 2010-07-20 3M Innovative Properties Company Flame resistant covercoat for flexible circuit
DE102006049519A1 (en) * 2006-10-20 2008-04-24 Lanxess Deutschland Gmbh Flame retardant for curable molding materials comprises ethylenediamine phosphate, a halogen-free phosphorus compound and a halogen-free nitrogen compound
KR20090067663A (en) * 2007-12-21 2009-06-25 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 Halogen-free flame retardant thermoplastic polyurethanes
EP2337892B1 (en) * 2008-08-15 2013-10-02 Otis Elevator Company Elevator system comprising a load bearing member with a nanoscale flame retardant and corresponding method of manufacturing said load bearing member
DE102010035103A1 (en) * 2010-08-23 2012-02-23 Catena Additives Gmbh & Co. Kg Flame retardant compositions containing triazine-intercalated metal phosphates
US10584230B2 (en) * 2013-11-21 2020-03-10 Dsm Ip Assets B.V. Flame-retardant polyamide composition
RU2556212C1 (en) * 2014-07-07 2015-07-10 Общество с ограниченной ответственностью "ТермоФасад" Composition for obtaining of fireproof polyurethane foam

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DD242941A (en) *
DE1694254C3 (en) * 1968-03-16 1984-06-28 Bayer Ag, 5090 Leverkusen Self-extinguishing fiber-reinforced polyamide molding compounds
DD143918A1 (en) * 1979-07-17 1980-09-17 Norbert Schubert METHOD FOR PRODUCING MODIFIED POLYAMIDE MOLD
JPS5945352A (en) * 1982-09-09 1984-03-14 Nissan Chem Ind Ltd Novel flame-retardant resin composition
JPS60144348A (en) * 1984-09-11 1985-07-30 Nissan Chem Ind Ltd Flame-retardant resin composition

Similar Documents

Publication Publication Date Title
JP3620852B2 (en) Method for producing melamine condensation product
US4325962A (en) Pharmaceutical compositions comprising a pyrazole derivative and method of use
CA1195329A (en) Alkylated polyalkylenepolyamines substituted oxo- piperazinyltriazines and uv light stabilized compositions
JP3341090B2 (en) Oxadiazole derivative and method for producing the same
CA1195327A (en) 1,2,4-triazine and pyrazine derivatives
JP2002540249A5 (en)
FR2725204A1 (en) 2-HYDROXYPHENYLTRIAZINES AS PHOTOSTABILIZING AGENTS
AU720041B2 (en) Method for the preparation of melamine
KR20000029661A (en) Method for the preparation of melamine
US4885316A (en) Substituted 5-amidotetrazoles as blowing agents in the production of cellular thermoplastic or rubber materials
NO175431B (en) Triazine based light stabilizers for plastics
JP4303426B2 (en) Flame retardant composition and process for producing the same
Takahashi et al. The Synthesis of 1, 3, 4-Benzotriazepin-5-one Derivatives from Isatoic Anhydrides
NO175432B (en) Melamine-based light stabilizers and plastics stabilized with these
NO982959L (en) Process for Modifying 1,3,5-Triazine Derivatives
US6410727B1 (en) Method for purifying melamine
Castro et al. Methiodide approach to the synthesis of 3-[2-(dimethylamino) ethyl]-5-[(1, 1-dioxo-5-methyl-1, 2, 5-thiadiazolidin-2-yl) methyl]-1H-indole and analogues
Okawa et al. A facile synthesis of 4 (3H)-pteridinone derivatives by utilizing N-{3-[(N-substituted) carbamoyl]-2-pyrazyl} iminophosphoranes
US2937172A (en) Alkoxxethylguanameses
JPH11292861A (en) Melamine cyanurate and its production
Elkaschef et al. Thio-acids—V: Some reactions of 3-oxo-1, 2-dithioles
Penieres et al. A new strategy for the synthesis of N-substituted 2, 5-dimethylpyrroles in heterogeneous medium.
HUP9701137A2 (en) Process for producing pharmaceutical intermedier
RU2187505C2 (en) 2-allylamino-4,6-bis-(ethoxycarboxylatomethyl-amino)-1,3,5-triazine as effective modifying agent-cohardening agent of epoxy oligomers in composites of anhydride hardening
JPH01153711A (en) Stabilization of oxymethylene copolymer