JPH11172111A - Modified asphalt composition for pavement - Google Patents

Modified asphalt composition for pavement

Info

Publication number
JPH11172111A
JPH11172111A JP36163197A JP36163197A JPH11172111A JP H11172111 A JPH11172111 A JP H11172111A JP 36163197 A JP36163197 A JP 36163197A JP 36163197 A JP36163197 A JP 36163197A JP H11172111 A JPH11172111 A JP H11172111A
Authority
JP
Japan
Prior art keywords
mass
molecular weight
asphalt
average molecular
styrene
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
JP36163197A
Other languages
Japanese (ja)
Other versions
JP4067161B2 (en
Inventor
Masaaki Kawatsuki
正明 川付
Seiya Tanaka
晴也 田中
Kiyomi Takagi
清美 高木
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
COSMO SOGO KENKYUSHO KK
Cosmo Oil Co Ltd
Original Assignee
COSMO SOGO KENKYUSHO KK
Cosmo Oil Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by COSMO SOGO KENKYUSHO KK, Cosmo Oil Co Ltd filed Critical COSMO SOGO KENKYUSHO KK
Priority to JP36163197A priority Critical patent/JP4067161B2/en
Publication of JPH11172111A publication Critical patent/JPH11172111A/en
Application granted granted Critical
Publication of JP4067161B2 publication Critical patent/JP4067161B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a modified asphalt composition for pavement that is excellent in viscosity at 60 deg.C and toughbess and has excellent storage stability at elevated temperatures. SOLUTION: The asphalt that satisfies the following formulae I and II and contains 0-30 mass% o asphalt fraction and 1-100 mass% of an aromatic fraction is modified by adding at least one of rubber, a thermiplastic elastomer and a resin as a modifier where the amount of the rubber, the thermiplastic elastomer or the resin as a modifier is set to 2-40 mass% based on the total of the asphalt and each modifier. Formula I:Z1>0.4 Z1=+3.07-3.28×MN /1,000-2.19×AS/AR Formula II:Z2>0.4 Z2=+0.14-2.95×AS/AR-1.5×MW /1,000+1.37×MW/MN (MN is number-average molecular weight; MW is weight average molecular weight, As is asphalt fraction mass%, AR is aromatic fraction mass%).

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、舗装用改質アスフ
ァルトに関するものである。さらに詳しくは、車道、歩
道、公園等にアスファルト舗装を行う際の密粒度混合物
を用いた通常舗装混合物あるいは開粒度混合物を用いた
排水性舗装に用いる改質アスファルトに関するものであ
る。
The present invention relates to a modified asphalt for pavement. More specifically, the present invention relates to a modified asphalt used for a normal pavement mixture using a dense particle mixture or a drainage pavement using an open particle mixture for asphalt pavement on a road, a sidewalk, a park, or the like.

【0002】[0002]

【従来の技術】道路舗装用のアスファルト材料として
は、ストレートアスファルト及び改質アスファルトが主
として用いられている。このうちストレートアスファル
トの性能を改善した改質アスファルトには、ストレート
アスファルトにゴム、熱可塑性エラストマーを単独、ま
たは両者を併用添加したゴム・熱可塑性エラストマー入
りアスファルトとストレートアスファルトを原料油と
し、高温下で空気を吹き込む操作、すなわちブローイン
グ操作を行うことにより、感温性を改善し、かつ60℃
における粘度を800から1200Pa・S(パスカル
秒)に高めたセミブローンアスファルトがある。ストレ
ートアスファルトに比べ、改質アスファルトは、重車両
交通によるわだちぼれやタイヤチェーン等による磨耗抵
抗性を高めており、アスファルト混合物性能の向上が図
られている。なかでも雨天時における舗装表面上の滞水
を防ぎ、自動車の高速走行時のハイドロプレーニング低
減効果や騒音低減効果の高い開粒度混合物に用いらる排
水性舗装用高粘度バインダーは、耐流動効果が高くなる
ように、60℃粘度を20000Pa・s以上、骨材と
の把握力を示す指標であるタフネス、テナシティに関し
ては、それぞれ20N・m以上、15N・m以上のよう
に改質アスファルト協会での規格は定められている。
2. Description of the Related Art Straight asphalt and modified asphalt are mainly used as asphalt materials for road pavement. Of these, asphalt with improved performance of straight asphalt, asphalt with rubber / thermoplastic elastomer and straight asphalt with rubber or thermoplastic elastomer added to straight asphalt alone or in combination with both, as raw oil, By performing an operation of blowing air, that is, a blowing operation, the temperature sensitivity is improved, and 60 ° C.
There is a semi-blown asphalt in which the viscosity is increased from 800 to 1200 Pa · S (Pascal second). Compared with straight asphalt, modified asphalt has improved resistance to abrasion caused by heavy vehicle traffic and abrasion caused by tire chains and the like, and the asphalt mixture performance has been improved. Above all, the high-viscosity binder for drainage pavement used in open-grain mixtures that prevent water accumulation on the pavement surface in rainy weather and have a high hydroplaning reduction effect and a high noise reduction effect during high-speed running of automobiles has a flow resistance effect. As high, the viscosity at 60 ° C is 20,000 Pa · s or more, and the toughness and tenacity, which are indicators of the grasping power with the aggregate, are 20 N · m or more and 15 N · m or more, respectively. Standards are defined.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、ゴム・
熱可塑性エラストマー入りアスファルトは、ゴム・熱可
塑性エラストマーの添加により60℃粘度、タフネス、
テナシティが増大するという改質効果があるものの、従
来のゴム・熱可塑性エラストマー入りアスファルトは、
ベースアスファルトと改質材との相溶性が十分でなく、
改質効果が低く、また、加熱貯蔵安定性が低下し、加熱
貯蔵時に膜を張る場合もあり、満足な効果が得られてい
なかった。
[Problems to be solved by the invention]
Asphalt containing thermoplastic elastomer has viscosity of 60 ° C, toughness,
Although there is a modifying effect that tenacity increases, conventional asphalt containing rubber and thermoplastic elastomer,
The compatibility between the base asphalt and the modifier is not sufficient,
The reforming effect was low, the storage stability under heating was reduced, and a film was sometimes formed during storage under heating, and a satisfactory effect was not obtained.

【0004】[0004]

【課題を解決するための手段】本発明者らは、上記課題
を解決するために鋭意検討を行った結果、特定の組成を
もち、かつ式(1)または(2)を満たすアスファルト
類に、特定な改質材を配合した舗装用改質アスファルト
組成物は、耐流動性としての指標である60℃粘度が高
く、さらに骨材の把握力を示す指標の1つであるタフネ
スが高く、さらには加熱貯蔵安定性が高いことを見いだ
し、本発明を完成するに至った。すなわち本発明は、式
(1)または式(2)を満たし、かつアスファルテン分
量が0〜30質量%、芳香族分量が1〜100質量%で
あるアスファルト類に、改質材として、ゴム、熱可塑性
エラストマー、及び樹脂のうち少なくとも1種が配合さ
れており、配合されているときのゴム、熱可塑性エラス
トマー、又は樹脂の含有量がそれぞれアスファルト類と
前記各改質材の合計量の2〜40質量%であることを特
徴とする舗装用改質アスファルト組成物を提供するもの
である。以下、本発明方法の詳細を作用と共に説明す
る。
Means for Solving the Problems The present inventors have conducted intensive studies in order to solve the above-mentioned problems, and as a result, asphalts having a specific composition and satisfying the formula (1) or (2), The modified asphalt composition for pavement containing a specific modifier has a high viscosity of 60 ° C., which is an index of the flow resistance, and a high toughness, which is one of the indexes showing the grasping power of the aggregate. Found that the heat storage stability was high, and completed the present invention. That is, the present invention relates to asphalts satisfying the formula (1) or the formula (2) and having an asphaltene content of 0 to 30% by mass and an aromatic content of 1 to 100% by mass. At least one of a plastic elastomer and a resin is blended, and the content of the rubber, the thermoplastic elastomer, or the resin when blended is 2 to 40 of the total amount of the asphalts and the respective modifiers. It is intended to provide a modified asphalt composition for pavement, characterized in that the composition is mass%. Hereinafter, the details of the method of the present invention will be described together with the operation.

【0005】[0005]

【発明の実施の形態】本発明で使用するアスファルト類
は、式(1)または式(2)を満たすアスファルト類で
あり、かつアスファルト類の組成が、アスファルト類の
全体量に対して、アスファルテン分が0〜30質量%、
好ましくは0〜20質量%であり、芳香族分が1〜10
0質量%、好ましくは10〜100質量%であるであ
る。アスファルテン分が30質量%を超える場合、ベー
スとなるアスファルト類が硬くなり過ぎ、低温ひび割れ
や施工性の面で好ましくない。また、アスファルテン分
のような高分子量成分が多過ぎると、改質材との相溶性
の面でも好ましくない。ベースとなるアスファルト類の
式(1)または式(2)におけるZ1、Z2値は0.4
を超えた値であるが、好ましくは0.4<Z1<3であ
り、0.4<Z2<5である。Z1、Z2が、0.4よ
り小さい場合、改質材を添加すると、改質材がアスファ
ルト中に島状に点在し、改質材の分散状態が低下し、改
質効果も小さく、加熱貯蔵時に膜を生成しやすいため好
ましくない。
BEST MODE FOR CARRYING OUT THE INVENTION The asphalts used in the present invention are asphalts satisfying the formula (1) or (2), and the composition of the asphalts is based on the asphaltene content with respect to the total amount of the asphalts. Is 0 to 30% by mass,
Preferably it is 0 to 20% by mass and the aromatic content is 1 to 10%.
0% by mass, preferably 10 to 100% by mass. If the asphaltene content exceeds 30% by mass, the asphalt base material becomes too hard, which is not preferable in terms of low-temperature cracking and workability. Further, if the amount of the high molecular weight component such as asphaltene is too large, it is not preferable in terms of compatibility with the modifier. The Z1 and Z2 values in the formula (1) or the formula (2) of the base asphalt are 0.4.
, But preferably 0.4 <Z1 <3 and 0.4 <Z2 <5. When Z1 and Z2 are smaller than 0.4, when the modifying agent is added, the modifying agent is scattered in the asphalt in an island shape, the dispersion state of the modifying agent is reduced, the modifying effect is small, and the heating is performed. It is not preferable because a film is easily formed during storage.

【0006】上記アスファルト類は、具体的には、例え
ば各種原油を常圧蒸留装置及び減圧蒸留装置にかけ、軽
質分を除去して得られる瀝青物質であるストレートアス
ファルト、原油を減圧蒸留した際の減圧蒸留留出油、溶
剤脱れきアスファルト、もしくはストレートアスファル
トを常圧下で230〜270℃の温度で空気を吹き込
み、構成している炭化水素に脱水素重合、縮合反応を起
こさせてコンシステンシーの高い状態にしたセミブロー
ンアスファルトやブローンアスファルト等が挙げられ
る。アスファルト類は、1種単独で用いても良いし、2
種以上を組み合わせて用いても良い。上記記載における
組成は、石油学会法(JPI−5S−22)による組成
分析試験結果であり、数平均分子量(MN)および重量
平均分子量(MW)は、ゲルパーミネーションクロマト
グラフィー(GPC)法で測定し、ポリスチレン換算で
求めた。
[0006] The asphalts described above include, for example, straight asphalt, which is a bituminous substance obtained by subjecting various crude oils to a normal pressure distillation apparatus and a reduced pressure distillation apparatus to remove light components, and a reduced pressure when the crude oil is distilled under reduced pressure. Air is blown at a temperature of 230 to 270 ° C. under normal pressure at a pressure of 230 to 270 ° C. by distilling distillate oil, solvent deasphalted asphalt, or straight asphalt, causing dehydrogenation polymerization and condensation reaction to occur in the constituent hydrocarbons, resulting in a state of high consistency. Semi-blown asphalt and blown asphalt. Asphalts may be used alone or as 2
A combination of more than one species may be used. The composition in the above description is the result of a composition analysis test according to the Japan Petroleum Institute method (JPI-5S-22), and the number average molecular weight (MN) and the weight average molecular weight (MW) are measured by gel permeation chromatography (GPC). And calculated in terms of polystyrene.

【0007】本発明の式において構成されるのは、アス
ファルテンと芳香族分の比だけではなく、分子量や分子
量の比または、両者の組み合わせにより構成されるもの
である。従って以下の組成や分子量に関する記述は、目
安となるものである。MW/MNは分子量分布の尺度と
なる値であり、その値が大きいほど、分子量分布が広い
と言える。故に、MW/MNが大きいものは、平均分子
量は小さくても、高分子量成分が多く存在する可能性が
ある。そして高分子量成分が多く存在すると、改質材の
分散状態が低下する。MW/MNの好ましい範囲は、1
〜5である。また、AS/ARは、改質材の溶解成分と
して重要な尺度である。その値が大きければ、すなわち
AR量に比べAS量が多くなる場合には、改質材を溶解
することができず、改質アスファルトとしての性状を示
さない。さらに、AS/ARが小さい場合、すなわち、
AS量に比べAR量が多い場合、改質材を溶解する効果
が高いため、改質材の分散がよくなる。AS/ARの好
ましい範囲は、0〜30であり、さらに好ましくは0〜
5である。
In the formula of the present invention, not only the ratio of asphaltenes and aromatic components, but also the molecular weight, the ratio of molecular weights, or a combination of both. Therefore, the following description regarding composition and molecular weight is only a guide. MW / MN is a value serving as a measure of the molecular weight distribution, and it can be said that the larger the value, the wider the molecular weight distribution. Therefore, those having a large MW / MN may have a large amount of high molecular weight components even though the average molecular weight is small. When a large amount of the high molecular weight component is present, the state of dispersion of the modifier is reduced. The preferred range of MW / MN is 1
~ 5. AS / AR is an important measure as a dissolved component of the modifier. If the value is large, that is, if the AS amount is larger than the AR amount, the modifying material cannot be dissolved, and does not exhibit properties as modified asphalt. Further, when AS / AR is small, that is,
When the AR amount is larger than the AS amount, the effect of dissolving the modifying material is high, so that the modifying material is well dispersed. The preferred range of AS / AR is 0 to 30, more preferably 0 to 30.
5

【0008】本発明の舗装用改質アスファルト組成物に
用いられる改質材としては、ゴム、熱可塑性エラストマ
ー及び樹脂が挙げられる。改質材は、1種単独、もしく
は2種以上を組み合わせて用いることができる。これら
の改質材の主な改質効果として、ゴムは伸度、熱可塑性
エラストマーは60℃粘度、タフネス、樹脂はタフネス
の各性状の改善効果がある。ゴムとしては、例えばクロ
ロプレンゴム、スチレン−ブタジエンゴム、天然ゴム等
が挙げられ、特に好ましくはスチレン−ブタジエンゴム
である。スチレン−ブタジエンゴムとしては、スチレン
を任意の割合で含有する種々のスチレン−ブタジエンゴ
ムが使用できるが、結合スチレン含有量が20〜30質
量%のものが好ましく、特にラテックス状であり、固形
分が45〜75質量%、固形分密度が0.92〜0.9
7g/cm3のものが好ましい。固形分が少な過ぎる
と、所要量を配合するための配合時間が長くなり、作業
性が低下する。逆に、固形分が多過ぎるとラテックスの
粘度が高くなり、均一な混合が難しくなる。また、結合
スチレン含有量が少ないと、60℃粘度等の上昇効果が
低減する傾向があり、結合スチレン含有量が多過ぎると
伸度に対する改善効果が低下する傾向がある。ゴムは、
1種単独で用いてもよいし、2種以上を組み合わせて用
いてもよい。
The modifier used in the modified asphalt composition for paving of the present invention includes rubber, thermoplastic elastomer and resin. The modifier may be used alone or in combination of two or more. As the main modifying effects of these modifiers, rubber has an effect of improving elongation, thermoplastic elastomer has a viscosity of 60 ° C., and toughness and resin have an effect of improving toughness. Examples of the rubber include chloroprene rubber, styrene-butadiene rubber, natural rubber and the like, and particularly preferably styrene-butadiene rubber. As the styrene-butadiene rubber, various styrene-butadiene rubbers containing styrene at an arbitrary ratio can be used, but those having a bound styrene content of 20 to 30% by mass are preferable, and are particularly latex-like and have a solid content of 45 to 75% by mass, solid content density of 0.92 to 0.9
7 g / cm 3 is preferred. If the solid content is too small, the compounding time for compounding the required amount becomes long, and the workability decreases. Conversely, if the solids content is too high, the viscosity of the latex increases, making uniform mixing difficult. Also, when the content of bound styrene is small, the effect of increasing the viscosity at 60 ° C. tends to decrease, and when the content of bound styrene is too large, the effect of improving elongation tends to decrease. Rubber is
One type may be used alone, or two or more types may be used in combination.

【0009】本発明に用いる熱可塑性エラストマーとし
ては、例えばスチレン−ブタジエン−スチレンブロック
共重合体、スチレン−イソプレン−スチレンブロック共
重合体、スチレン−エチレン−ブタジエン−スチレンブ
ロック共重合体等が挙げられ、好ましくはスチレン−ブ
タジエン−スチレンブロック共重合体が挙げられる。こ
れらのスチレン共重合体のスチレン量は、20〜50質
量%が好ましく、特に30〜45質量%が好ましい。ス
チレン量が少な過ぎると、タフネス、60℃粘度の改善
効果が低下し、また、スチレン含有が多過ぎると、ベー
スアスファルトとの相溶性が低下する傾向がある。さら
に、この熱可塑性エラストマーの重量平均分子量は、5
0,000〜500,000の範囲が好ましく、特に1
00,000〜300,000の範囲が好ましい。重量
平均分子量が小さ過ぎると、改質効果が小さく、大量の
配合が必要となる。逆に、重量平均分子量が大き過ぎる
と、ベースアスファルトとの相溶性が低下する傾向があ
る。熱可塑性エラストマーは、1種単独で用いてもよい
し、2種以上を組み合わせて用いてもよい。
The thermoplastic elastomer used in the present invention includes, for example, styrene-butadiene-styrene block copolymer, styrene-isoprene-styrene block copolymer, styrene-ethylene-butadiene-styrene block copolymer, and the like. Preferably, a styrene-butadiene-styrene block copolymer is used. The styrene content of these styrene copolymers is preferably from 20 to 50% by mass, particularly preferably from 30 to 45% by mass. If the amount of styrene is too small, the effect of improving the toughness and the viscosity at 60 ° C. decreases, and if the amount of styrene is too large, the compatibility with the base asphalt tends to decrease. Further, the weight average molecular weight of this thermoplastic elastomer is 5
The range is preferably from 000 to 500,000, particularly preferably 1 to 500.
The range of 00,000 to 300,000 is preferred. If the weight average molecular weight is too small, the modifying effect is small and a large amount of compounding is required. Conversely, if the weight average molecular weight is too large, the compatibility with the base asphalt tends to decrease. The thermoplastic elastomers may be used alone or in combination of two or more.

【0010】本発明に用いる樹脂は、脂肪族系炭化水素
樹脂、脂環族系炭化水素樹脂、水素添加炭化水素樹脂等
の熱可塑性をもつ石油樹脂類が好ましい。また、石油樹
脂類の軟化点は、70〜150℃で、好ましくは80℃
〜145℃である。軟化点が低過ぎると、改質効果が小
さく、また逆に軟化点が高過ぎるとアスファルトが硬く
なり過ぎ、施工性等の面で問題が生じるおそれがある。
さらに、石油樹脂類の数平均分子量(MN)は200〜
1500、重量平均分子量(MW)は300〜3000
の範囲が好ましく、特にMNが300〜1300、MW
が400〜2,800の範囲が好ましい。MN及びMW
が小さ過ぎると、改質効果が小さく、大量の配合が必要
となり、逆にMN及びMWが大き過ぎると、相溶性が低
下するおそれがある。樹脂は、1種単独で用いてもよい
し、2種以上を組み合わせて用いてもよい。各種改質材
の数平均分子量及び重量平均分子量はGPC法で測定
し、ポリスチレン換算で求めたものである。
The resin used in the present invention is preferably a petroleum resin having thermoplasticity such as an aliphatic hydrocarbon resin, an alicyclic hydrocarbon resin, or a hydrogenated hydrocarbon resin. The softening point of petroleum resins is 70 to 150 ° C, preferably 80 ° C.
14145 ° C. If the softening point is too low, the modifying effect is small, and if the softening point is too high, the asphalt becomes too hard, which may cause problems in workability and the like.
Further, the number average molecular weight (MN) of petroleum resins is 200 to
1500, weight average molecular weight (MW) 300-3000
Is preferable, and especially MN is 300 to 1300 and MW
Is preferably in the range of 400 to 2,800. MN and MW
Is too small, the modifying effect is small, and a large amount of compounding is required. Conversely, if MN and MW are too large, the compatibility may be reduced. One type of resin may be used alone, or two or more types may be used in combination. The number average molecular weight and the weight average molecular weight of the various modifiers were measured by GPC and determined in terms of polystyrene.

【0011】改質材の含有量は、アスファルト類と各改
質材の合計量に対して、それぞれ2〜40質量%であ
り、好ましくは3〜30質量%である。具体的には、改
質材としてゴムが配合されている場合、ゴムの含有量
は、アスファルト類とゴムの合計量に対して、2〜40
質量%であり、好ましくは3〜30質量%である。ま
た、改質材として熱可塑性エラストマーが配合されてい
る場合、熱可塑性エラストマーの含有量は、アスファル
ト類と熱可塑性エラストマーの合計量に対して、2〜4
0質量%であり、好ましくは3〜30質量%である。さ
らに、改質材として樹脂が配合されている場合、樹脂の
含有量は、アスファルト類と樹脂の合計量に対して、2
〜40質量%であり、好ましくは3〜30質量%であ
る。これらの含有量が2質量%を下回るほど少ない場
合、改質効果が小さくなり、また40質量%を超えるほ
ど多くなると、高温時の動粘度が高くなるため、骨材と
の混合性が低下する傾向がある。
The content of the modifier is 2 to 40% by mass, preferably 3 to 30% by mass, based on the total amount of asphalts and each modifier. Specifically, when rubber is compounded as a modifier, the content of rubber is 2 to 40 with respect to the total amount of asphalts and rubber.
%, Preferably 3 to 30% by mass. When a thermoplastic elastomer is blended as a modifier, the content of the thermoplastic elastomer is 2 to 4 with respect to the total amount of the asphalts and the thermoplastic elastomer.
0 mass%, preferably 3 to 30 mass%. Further, when a resin is blended as a modifier, the content of the resin is 2% of the total amount of the asphalts and the resin.
-40% by mass, preferably 3-30% by mass. When the content is less than 2% by mass, the modifying effect is reduced. When the content is more than 40% by mass, the kinematic viscosity at high temperature is increased, and the mixing property with the aggregate is reduced. Tend.

【0012】本発明の舗装用改質アスファルト組成物
は、上記各成分を所定割合で配合することにより製造す
ることができる。各成分の配合順序は、特に制限されな
いが、ベース基材を混合した後、樹脂、熱可塑性エラス
トマー、あるいはゴム等の順序で改質材を配合すること
が好ましい。ベース基材へのゴム、熱可塑性エラストマ
ー等の混合は、プロペラ式攪拌機、ホモミキサー等の各
種攪拌機が使用できるが、高せん断力をかけるホモミキ
サーが好ましい。ただし、石油樹脂の場合は、熱をかけ
るだけで溶解混合するので、必ずしも高せん断力をかけ
る必要はない。各成分の混合温度は、特に制限されるも
のではないが、通常150〜200℃で行うことができ
る。また、混合時間も特に制限されるものではないが、
通常改質材1成分につき5分〜10時間、好ましくは1
0分〜5時間である。
The modified asphalt composition for pavement of the present invention can be produced by mixing the above components at a predetermined ratio. The order of blending the components is not particularly limited, but it is preferable to blend the modifier in the order of resin, thermoplastic elastomer, rubber or the like after mixing the base material. Various agitators such as a propeller-type agitator and a homomixer can be used for mixing the rubber, the thermoplastic elastomer, and the like into the base material, but a homomixer that applies a high shear force is preferable. However, in the case of petroleum resin, it is not always necessary to apply a high shearing force because it is melted and mixed only by applying heat. The mixing temperature of each component is not particularly limited, but the mixing can be usually performed at 150 to 200 ° C. Also, the mixing time is not particularly limited,
Usually 5 minutes to 10 hours, preferably 1 to 1 component of modifier
0 minutes to 5 hours.

【0013】本発明の舗装用改質アスファルト組成物
は、必要により、通常舗装用改質アスファルトに添加さ
れる他の添加剤、例えば剥離防止剤、分散剤、安定剤な
どを添加してもよい。また、可塑剤を配合して調製する
ことも可能であり、例えば、常圧残査油、減圧残査油、
減圧蒸留留出油、溶剤脱瀝油、ベースオイル、芳香族油
等が挙げられる。可塑剤は1種単独で用いてもよいし、
2種以上を組み合わせて用いてもよい。
[0013] The modified asphalt composition for pavement of the present invention may, if necessary, contain other additives usually added to the modified asphalt for pavement, such as an anti-stripping agent, a dispersant and a stabilizer. . It is also possible to blend and prepare a plasticizer, for example, normal pressure residual oil, reduced pressure residual oil,
Vacuum distillation distillate, solvent deasphalted oil, base oil, aromatic oil and the like. One type of plasticizer may be used alone,
Two or more kinds may be used in combination.

【0014】また、本発明の舗装用改質アスファルト組
成物の施工方法は、舗装用改質アスファルト組成物を所
定の温度で骨材、フィラー等と混合し、舗装場所に敷設
し、転圧することにより行うことができる。骨材、フィ
ラー等との混合温度は、通常の混合温度でよく、例えば
165〜185℃でよい。また、転圧時の温度は通常の
転圧温度でよく、例えば150〜175℃でよい。
Further, the method for applying the modified asphalt composition for pavement of the present invention comprises mixing the modified asphalt composition for pavement with an aggregate, a filler or the like at a predetermined temperature, laying the mixture on a pavement site, and compacting it. Can be performed. The mixing temperature with the aggregate, the filler and the like may be a normal mixing temperature, for example, 165 to 185 ° C. The rolling temperature may be a normal rolling temperature, for example, 150 to 175 ° C.

【0015】[0015]

【実施例】次に、本発明を実施例、及び比較例によりさ
らに具体的に説明する。なお、本発明は、これらの例に
よって何ら制限されるものではない。実施例、比較例に
おける軟化点、針入度、伸度はJIS K2207に、
60℃粘度、及びタフネスは舗装試験法便覧((社)日
本道路協会、昭和63年版)に準拠して行った。改質ア
スファルトの加熱貯蔵安定性は、約200gの改質アス
ファルトを、350mlのアルミ缶に入れ、160℃×
7日間で加熱し、表面一面に改質材の膜が張っているも
のを安定性×、膜張りが全くないか、もしくは少ないも
のを安定性○とした。また、組成分析は石油学会法(J
PI−5S−22)に準拠して行い、数平均分子量(M
N)および重量平均分子量(MW)はゲル浸透クロマト
グラフィ(GPC)により測定し、ポリスチレン換算で
求めた。GPC測定は、TOSOHHLC−8120の
装置により、テトラヒドロフラン(THF)を移動相と
して、TSKgel SuperHM−Nカラムを用い
て行った。
Next, the present invention will be described more specifically with reference to examples and comparative examples. The present invention is not limited by these examples. The softening point, penetration and elongation in Examples and Comparative Examples are based on JIS K2207.
The viscosity at 60 ° C. and the toughness were determined in accordance with the Handbook of Pavement Testing Method (Japan Road Association, 1988). Heat storage stability of the modified asphalt was measured by placing about 200 g of the modified asphalt in a 350 ml aluminum can,
The film was heated for 7 days, and the surface of the surface of which the modifier was covered was designated as stability x, and the film having no or little film coverage was designated as stability ○. The composition analysis is based on the Japan Petroleum Institute method (J
PI-5S-22), the number average molecular weight (M
N) and the weight average molecular weight (MW) were measured by gel permeation chromatography (GPC), and were determined in terms of polystyrene. The GPC measurement was performed using a TSKgel Super HM-N column with tetrahydrofuran (THF) as a mobile phase using an apparatus of TOSOOH HLC-8120.

【0016】実施例1 式(1)を満たすZ1=0.52(数平均分子量(M
N)610、AS=10.6質量%、AR=42.3質
量%、AS/AR=0.25)のストレートアスファル
トに、スチレン−ブタジエン−スチレンブロック共重合
体熱可塑性エラストマー(SBS、スチレン/ブタジエ
ン重合比:40/60、重量平均分子量:150,00
0)を、ストレートアスファルトとSBSの合計量の6
質量%を配合し、高せん断力のホモミキサーを用いて、
180℃×2時間で混合し、改質アスファルト組成物を
得た。表1に得られた組成物の性状を示す。
Example 1 Z1 = 0.52 (number average molecular weight (M
N) 610, AS = 10.6% by mass, AR = 42.3% by mass, AS / AR = 0.25) on a styrene-butadiene-styrene block copolymer thermoplastic elastomer (SBS, styrene / Butadiene polymerization ratio: 40/60, weight average molecular weight: 150,000
0) is 6 of the total amount of straight asphalt and SBS
% By mass and using a high shear homomixer.
The mixture was mixed at 180 ° C. for 2 hours to obtain a modified asphalt composition. Table 1 shows the properties of the obtained composition.

【0017】実施例2 式(1)を満たすZ1=0.44(数平均分子量(M
N)620、AS=12.1質量%、AR=44.1質
量%、AS/AR=0.27)のストレートアスファル
トに、軟化点125℃、数平均分子量(MN)450、
重量平均分子量(MW)720の石油樹脂をストレート
アスファルトと石油樹脂の合計量の25質量%、170
℃×30分において混合し、スチレン−ブタジエン−ス
チレンブロック共重合体熱可塑性エラストマー(SB
S、スチレン/ブタジエン重合比:40/60、重量平
均分子量:150,000)を、ストレートアスファル
トとSBSの合計量の8質量%、高せん断力のホモミキ
サーを用いて、180℃×2時間で混合し、改質アスフ
ァルト組成物を得た。表1に得られた組成物の性状を示
す。
Example 2 Z1 = 0.44 (number average molecular weight (M
N) 620, AS = 12.1 mass%, AR = 44.1 mass%, AS / AR = 0.27), a softening point of 125 ° C., a number average molecular weight (MN) of 450,
A petroleum resin having a weight average molecular weight (MW) of 720 was converted to 25% by mass of the total amount of the straight asphalt and the petroleum resin.
Styrene-butadiene-styrene block copolymer thermoplastic elastomer (SB
S, styrene / butadiene polymerization ratio: 40/60, weight average molecular weight: 150,000) at 180 ° C. × 2 hours using a homomixer with a high shearing force of 8% by mass of the total amount of straight asphalt and SBS. After mixing, a modified asphalt composition was obtained. Table 1 shows the properties of the obtained composition.

【0018】実施例3 式(1)を満たすZ1=1.09(数平均分子量(M
N)570、AS=2.6質量%、AR=51.7%、
AS/AR=0.05)のストレートアスファルトに、
Z1=0.36の減圧残査油(MN=680、AS=
4.8質量%、AR=21.8質量%、AS/AR=
0.22)を全体量の20%添加し、式(1)を満たす
Z1=0.98(MN=590、AS=3.0質量%、
AR=42.5質量%、AS/AR=0.07)のアス
ファルトを調製し、軟化点125℃、数平均分子量(M
N)450、重量平均分子量(MW)720の石油樹脂
をアスファルトと石油樹脂の合計量の20質量%、17
0℃×30分において混合し、スチレン−ブタジエン−
スチレンブロック共重合体熱可塑性エラストマー(SB
S、スチレン/ブタジエン重合比:40/60、重量平
均分子量:150,000)を、アスファルトとSBS
の合計量の6質量%、高せん断力のホモミキサーを用い
て、180℃×2時間で混合し、改質アスファルト組成
物を得た。表1に得られた組成物の性状を示す。
Example 3 Z1 = 1.09 (number average molecular weight (M
N) 570, AS = 2.6% by mass, AR = 51.7%,
AS / AR = 0.05) on straight asphalt
Vacuum residue of Z1 = 0.36 (MN = 680, AS =
4.8% by mass, AR = 21.8% by mass, AS / AR =
0.22) was added at 20% of the total amount, and Z1 = 0.98 (MN = 590, AS = 3.0% by mass) satisfying the expression (1).
AR = 42.5% by mass, AS / AR = 0.07) was prepared, the softening point was 125 ° C., and the number average molecular weight (M
N) 450, a petroleum resin having a weight average molecular weight (MW) 720 of 20% by mass of the total amount of asphalt and petroleum resin,
Mix at 0 ° C. for 30 minutes and mix styrene-butadiene-
Styrene block copolymer thermoplastic elastomer (SB
S, styrene / butadiene polymerization ratio: 40/60, weight-average molecular weight: 150,000), asphalt and SBS
6% by mass of the total amount was mixed at 180 ° C. for 2 hours using a homomixer having a high shearing force to obtain a modified asphalt composition. Table 1 shows the properties of the obtained composition.

【0019】実施例4 式(2)を満たすZ2=1.09(数平均分子量(M
N)540、重量平均分子量(MW)1240、AS=
4.6質量%、AR=46.6質量%、AS/AR=
0.10)のストレートアスファルトに、Z2=0.3
1の減圧残査油(MN=680 MW=2000、AS
=8.8質量%、AR=33.8質量%、AS/AR=
0.26)を全体量の20%添加し、式(2)を満たす
Z=0.91(MN=580、MW=1380、AS=
4.8質量%、AR=40.8質量%、AS/AR=
0.12)のアスファルトを調製し、軟化点125℃、
数平均分子量(MN)450、重量平均分子量(MW)
720の石油樹脂をアスファルトと石油樹脂の合計量の
20質量%、170℃×30分において混合し、スチレ
ン−ブタジエン−スチレンブロック共重合体熱可塑性エ
ラストマー(SBS、スチレン/ブタジエン重合比:4
0/60、重量平均分子量:150,000)を、アス
ファルトとSBSの合計量の8質量%、高せん断力のホ
モミキサーを用いて、180℃×2時間で混合し、改質
アスファルト組成物を得た。表2に得られた組成物の性
状を示す。
Example 4 Z2 = 1.09 (number average molecular weight (M
N) 540, weight average molecular weight (MW) 1240, AS =
4.6% by mass, AR = 46.6% by mass, AS / AR =
0.10) on straight asphalt, Z2 = 0.3
1 vacuum residue (MN = 680 MW = 2000, AS
= 8.8% by mass, AR = 33.8% by mass, AS / AR =
0.26) was added at 20% of the total amount, and Z = 0.91 (MN = 580, MW = 1380, AS =
4.8% by mass, AR = 40.8% by mass, AS / AR =
0.12) asphalt was prepared, and the softening point was 125 ° C.
Number average molecular weight (MN) 450, weight average molecular weight (MW)
No. 720 petroleum resin was mixed at 170 ° C. for 30 minutes at 20% by mass of the total amount of asphalt and petroleum resin, and a styrene-butadiene-styrene block copolymer thermoplastic elastomer (SBS, styrene / butadiene polymerization ratio: 4
0/60, weight average molecular weight: 150,000) was mixed at 180 ° C. for 2 hours using a high-shear homomixer at 8% by mass of the total amount of asphalt and SBS to obtain a modified asphalt composition. Obtained. Table 2 shows the properties of the obtained composition.

【0020】実施例5 式(2)を満たす Z2=0.63(数平均分子量(M
N)620、重量平均分子量(MW)1650、AS=
9.6質量%、AR=46.3質量%、AS/AR=
0.21)のストレートアスファルトに、スチレン−ブ
タジエン−スチレンブロック共重合体熱可塑性エラスト
マー(SBS、スチレン/ブタジエン重合比:40/6
0、重量平均分子量:150,000)を、ストレート
アスファルトとSBSの合計量の5質量%、高せん断力
のホモミキサーを用いて、180℃×2時間で混合し、
改質アスファルト組成物を得た。表2に得られた組成物
の性状を示す。
Example 5 Z2 = 0.63 (number average molecular weight (M
N) 620, weight average molecular weight (MW) 1650, AS =
9.6% by mass, AR = 46.3% by mass, AS / AR =
Styrene-butadiene-styrene block copolymer thermoplastic elastomer (SBS, styrene / butadiene polymerization ratio: 40/6)
0, weight average molecular weight: 150,000) at 180 ° C. for 2 hours using a high shear homomixer at 5% by mass of the total amount of straight asphalt and SBS,
A modified asphalt composition was obtained. Table 2 shows the properties of the obtained composition.

【0021】実施例6 式(2)を満たす Z2=0.91(数平均分子量(M
N)620、重量平均分子量(MW)1630、AS=
5.2質量%、AR=47.9質量%、AS/AR=
0.11)のストレートアスファルトに、軟化点125
℃、数平均分子量(MN)450、重量平均分子量(M
W)720の石油樹脂をストレートアスファルトと石油
樹脂の合計量の25質量%、170℃×30分において
混合しスチレン−ブタジエン−スチレンブロック共重合
体熱可塑性エラストマー(SBS、スチレン/ブタジエ
ン重合比:40/60、重量平均分子量:150,00
0)を、ストレートアスファルトとSBSの合計量の1
0質量%、高せん断力のホモミキサーを用いて、180
℃×2時間で混合し、改質アスファルト組成物を得た。
表2に得られた組成物の性状を示す。
Example 6 Z2 = 0.91 (number average molecular weight (M
N) 620, weight average molecular weight (MW) 1630, AS =
5.2% by mass, AR = 47.9% by mass, AS / AR =
0.11) Straightening asphalt with a softening point of 125
° C, number average molecular weight (MN) 450, weight average molecular weight (M
W) 720 petroleum resins were mixed at 25% by mass of the total amount of straight asphalt and petroleum resin at 170 ° C. for 30 minutes, and styrene-butadiene-styrene block copolymer thermoplastic elastomer (SBS, styrene / butadiene polymerization ratio: 40) / 60, weight average molecular weight: 150,000
0) is 1 of the total amount of straight asphalt and SBS
0% by mass, using a high shear homomixer, 180
The mixture was mixed at a temperature of 2 ° C. for 2 hours to obtain a modified asphalt composition.
Table 2 shows the properties of the obtained composition.

【0022】実施例7 式(2)を満たす Z2=0.57(数平均分子量(M
N)660、重量平均分子量(MW)1710、AS=
7.3質量%、AR=44.7質量%、AS/AR=
0.16)のストレートアスファルトに、軟化点125
℃、数平均分子量(MN)450、重量平均分子量(M
W)720の石油樹脂をストレートアスファルトと石油
樹脂の合計量の10質量%、170℃×30分において
混合しスチレン−ブタジエン−スチレンブロック共重合
体熱可塑性エラストマー(SBS、スチレン/ブタジエ
ン重合比:40/60、重量平均分子量:150,00
0)を、ストレートアスファルトとSBSの合計量の6
質量%、高せん断力のホモミキサーを用いて、180℃
×2時間で混合し、改質アスファルト組成物を得た。表
2に得られた組成物の性状を示す。
Example 7 Z2 = 0.57 (number average molecular weight (M
N) 660, weight average molecular weight (MW) 1710, AS =
7.3% by mass, AR = 44.7% by mass, AS / AR =
0.16) straight asphalt with a softening point of 125
° C, number average molecular weight (MN) 450, weight average molecular weight (M
W) 720 petroleum resins were mixed at 170 ° C. for 30 minutes at 10% by mass of the total amount of straight asphalt and petroleum resin, and styrene-butadiene-styrene block copolymer thermoplastic elastomer (SBS, styrene / butadiene polymerization ratio: 40) / 60, weight average molecular weight: 150,000
0) is 6 of the total amount of straight asphalt and SBS
Mass%, using a homo-mixer with high shearing force, 180 ° C
× 2 hours to obtain a modified asphalt composition. Table 2 shows the properties of the obtained composition.

【0023】比較例1 式(1)においてZ1=0.20(数平均分子量(M
N)680、AS= 13.2質量%、AR=45.2
質量%、AS/AR=0.29)を示すストレートアス
ファルトに、スチレン−ブタジエン−スチレンブロック
共重合体熱可塑性エラストマー(SBS、スチレン/ブ
タジエン重合比:40/60、重量平均分子量:15
0,000)を、ストレートアスファルトとSBSの合
計量の6質量%、高せん断力のホモミキサーを用いて、
180℃×2時間で混合し、改質アスファルト組成物を
得た。表1に得られた組成物の性状を示す。
Comparative Example 1 In the formula (1), Z1 = 0.20 (number average molecular weight (M
N) 680, AS = 13.2% by mass, AR = 45.2
Mass%, AS / AR = 0.29), styrene-butadiene-styrene block copolymer thermoplastic elastomer (SBS, styrene / butadiene polymerization ratio: 40/60, weight average molecular weight: 15)
0,000) with 6% by mass of the total amount of straight asphalt and SBS using a high shear homomixer.
The mixture was mixed at 180 ° C. for 2 hours to obtain a modified asphalt composition. Table 1 shows the properties of the obtained composition.

【0024】比較例2 式(1)においてZ1=−0.02(数平均分子量(M
N)710、AS=15.7質量%、AR=45.4質
量%、AS/AR=0.35)を示すストレートアスフ
ァルトに、軟化点125℃、数平均分子量(MN)45
0、重量平均分子量(MW)720の石油樹脂をストレ
ートアスファルトと石油樹脂の合計量の25質量%、1
70℃×30分において混合し、スチレン−ブタジエン
−スチレンブロック共重合体熱可塑性エラストマー(S
BS、スチレン/ブタジエン重合比:40/60、重量
平均分子量:150,000)を、ストレートアスファ
ルトとSBSの合計量の8質量%、高せん断力のホモミ
キサーを用いて、180℃×2時間で混合し、改質アス
ファルト組成物を得た。表1に得られた組成物の性状を
示す。
Comparative Example 2 In the formula (1), Z1 = −0.02 (number average molecular weight (M
N) 710, AS = 15.7% by mass, AR = 45.4% by mass, AS / AR = 0.35), softening point 125 ° C., number average molecular weight (MN) 45
0, 25 mass% of the total amount of petroleum resin having a weight average molecular weight (MW) of 720
The mixture was mixed at 70 ° C. for 30 minutes to form a styrene-butadiene-styrene block copolymer thermoplastic elastomer (S
BS, styrene / butadiene polymerization ratio: 40/60, weight average molecular weight: 150,000) at 180 ° C. for 2 hours using a homomixer with a high shearing force of 8% by mass of the total amount of straight asphalt and SBS. After mixing, a modified asphalt composition was obtained. Table 1 shows the properties of the obtained composition.

【0025】比較例3 式(2)においてZ2=0.18(数平均分子量(M
N)770、重量平均分子量(MW)2240、AS=
8.4質量%、AR=49.8質量%、AS/AR=
0.17)を示すストレートアスファルトに、軟化点1
25℃、数平均分子量(MN)450、重量平均分子量
(MW)720の石油樹脂をストレートアスファルトと
石油樹脂の合計量の5質量%、170℃×30分におい
て混合し、スチレン−ブタジエン−スチレンブロック共
重合体熱可塑性エラストマー(SBS、スチレン/ブタ
ジエン重合比:40/60、重量平均分子量:150,
000)を、ストレートアスファルトとSBSの合計量
の6質量%、高せん断力のホモミキサーを用いて、18
0℃×2時間で混合し、改質アスファルト組成物を得
た。表2に得られた組成物の性状を示す。
Comparative Example 3 In the formula (2), Z2 = 0.18 (number average molecular weight (M
N) 770, weight average molecular weight (MW) 2240, AS =
8.4% by mass, AR = 49.8% by mass, AS / AR =
0.17) to a soft asphalt of 1
A petroleum resin having a number average molecular weight (MN) of 450 and a weight average molecular weight (MW) of 720 was mixed at 5% by mass of the total amount of straight asphalt and petroleum resin at 170 ° C. for 30 minutes at 25 ° C., and a styrene-butadiene-styrene block was obtained. Copolymer thermoplastic elastomer (SBS, styrene / butadiene polymerization ratio: 40/60, weight average molecular weight: 150,
000) to 6% by mass of the total amount of straight asphalt and SBS using a high-shear homomixer.
The mixture was mixed at 0 ° C. × 2 hours to obtain a modified asphalt composition. Table 2 shows the properties of the obtained composition.

【0026】比較例4 式(2)においてZ2=0.23(数平均分子量(M
N)850、重量平均分子量(MW)2370、AS=
1.3質量%、AR=48.0質量%、AS/AR=
0.03)を示すストレートアスファルトに、軟化点1
25℃、数平均分子量(MN)450、重量平均分子量
(MW)720の石油樹脂をストレートアスファルトと
石油樹脂の合計量の20質量%、170℃×30分にお
いて混合し、スチレン−ブタジエン−スチレンブロック
共重合体熱可塑性エラストマー(SBS、スチレン/ブ
タジエン重合比:40/60、重量平均分子量:15
0,000)を、ストレートアスファルトとSBSの合
計量の8質量%、高せん断力のホモミキサーを用いて、
180℃×2時間で混合し、改質アスファルト組成物を
得た。表2に得られた組成物の性状を示す。
Comparative Example 4 In the formula (2), Z2 = 0.23 (number average molecular weight (M
N) 850, weight average molecular weight (MW) 2370, AS =
1.3% by mass, AR = 48.0% by mass, AS / AR =
0.03) to a soft asphalt of 1
A petroleum resin having a number average molecular weight (MN) of 450 and a weight average molecular weight (MW) of 720 was mixed at 25 ° C, 20% by mass of the total amount of the straight asphalt and the petroleum resin at 170 ° C for 30 minutes, and a styrene-butadiene-styrene block was obtained. Copolymer thermoplastic elastomer (SBS, styrene / butadiene polymerization ratio: 40/60, weight average molecular weight: 15
000) using 8% by mass of the total amount of straight asphalt and SBS using a high shear homomixer.
The mixture was mixed at 180 ° C. for 2 hours to obtain a modified asphalt composition. Table 2 shows the properties of the obtained composition.

【0027】[0027]

【表1】 [Table 1]

【0028】[0028]

【表2】 [Table 2]

【0029】実施例1では、改質材として、SBSを6
質量%混合した、実施例1と比較例1においては、ベー
スとなるアスファルトの数式(1)のZ1値0.4以上
を満たす実施例1は、SBSの分散状態が良好で、加熱
貯蔵時における膜張りは認められなかった。また改質効
果性状としての60℃粘度、タフネス、軟化点の改質効
果も大きい。一方、ベースとなるアスファルト類の式
(1)のZ1値0.4以上を満足しない比較例1は、S
BSの分散状態が不良であり、加熱貯蔵時における膜張
りが認められ、改質効果も実施例1ほどは得られていな
い。改質材として、SBSを8質量%、石油樹脂を25
質量%混合した、実施例2と比較例2においては、ベー
スとなるアスファルトの式(1)のZ1値0.4以上を
満たす実施例2は、SBSの分散状態が良好で、加熱貯
蔵時における膜張りは認められず、さらに軟化点、タフ
ネス、60℃粘度に関して、比較例2と比べて改質効果
も大きい。
In Example 1, SBS was used as a modifying material in 6 parts.
In Example 1 and Comparative Example 1 in which the mass% was mixed, Example 1 which satisfied the Z1 value of 0.4 or more in the formula (1) of the base asphalt had a good dispersion state of SBS, No filming was observed. The effect of modifying the viscosity at 60 ° C., toughness and softening point as properties of the modifying effect is also large. On the other hand, Comparative Example 1, which does not satisfy the Z1 value of 0.4 or more in the formula (1) of the base asphalt,
The dispersion state of the BS was poor, film sticking was observed during storage under heating, and the reforming effect was not obtained as in Example 1. 8% by mass of SBS and 25 of petroleum resin as modifiers
In Example 2 and Comparative Example 2 in which the mass% was mixed, Example 2 which satisfied the Z1 value of 0.4 or more in the formula (1) of the base asphalt had a good dispersion state of SBS, No film tension was observed, and the effect of modifying the softening point, toughness, and viscosity at 60 ° C. was greater than that of Comparative Example 2.

【0030】式(1)のZ1値0.4以上を満足するZ
1値が0.653となる実施例3に関しては、SBS6
質量%と石油樹脂20質量%だけでは改質効果が得られ
なかったため、可塑剤として減圧残査油を20質量%配
合した。本実施例3がもっともSBSの分散状態が優
れ、60℃粘度も高く、加熱貯蔵時の膜張りも認められ
なかった。請求項1の発明では、アスファルト類を説明
する指標として、分子量のほかにAS/ARなる指標を
併せて用いた結果、多変量解析の決定係数が分子量のみ
を用いた回帰式での0.82から0.92に上昇した。
これは、アスファルトの改質効果、加熱貯蔵安定性に分
子量だけではなく、AS/ARつまりアスファルト組成
における改質材の溶解成分としての芳香族分と溶解阻害
成分としてのアスファルテン分の比が寄与しているため
と思われる。
Z satisfying the Z1 value of 0.4 or more in equation (1)
For Example 3 in which one value is 0.653, SBS6
Since the modifying effect was not obtained only by 20% by mass and 20% by mass of petroleum resin, 20% by mass of a vacuum residue oil was blended as a plasticizer. In Example 3, the dispersion state of SBS was the most excellent, the viscosity was high at 60 ° C., and no film sticking was observed during heating and storage. According to the first aspect of the present invention, as an index for explaining asphalts, in addition to the molecular weight, an index of AS / AR is used. As a result, the coefficient of determination of the multivariate analysis is 0.82 in a regression equation using only the molecular weight. From 0.92 to 0.92.
This is because not only the molecular weight but also the ratio of the aromatic component as the dissolving component of the asphalt composition and the asphaltene component as the dissolution inhibiting component in the asphalt composition contribute to the asphalt modifying effect and the heat storage stability. It seems to be because.

【0031】請求項2の発明では、アスファルト類を説
明する指標として、MN,MW、MW/MN、AS/A
Rの指標を用いた。多変量解析の決定係数はさらに0.
94に上昇した。これは、MW/MNすなわち分子量分
布の尺度となる値が大きいほど、分子量分布が広いと言
えるが、MW/MNの値が大きいものは、平均分子量は
小さくても、高分子量成分が多く存在する可能性があ
り、高分子量成分が多く存在すると、改質材の分散状態
が低下することになる。このために数式の中に分子量の
比すなわち分子量分布を取り入れることにより決定係数
は向上した。特に比較例6に示すアスファルトでは、A
S/AR=0.03と非常に小さな値を示し、改質材の
溶解成分が多く、溶解阻害成分が少ないにも関わらず、
貯蔵安定性や改質効果が実施例4〜7に比べて劣ってい
るのは分子量や分子量分布が原因となっているためと考
えられる。
According to the second aspect of the present invention, MN, MW, MW / MN, AS / A are used as indices for explaining asphalts.
The index of R was used. The coefficient of determination of the multivariate analysis is also 0.
It rose to 94. This means that the molecular weight distribution is wider as the value of MW / MN, that is, the value that is a measure of the molecular weight distribution, is larger. However, those with a higher value of MW / MN have more high molecular weight components even though the average molecular weight is smaller. If there is a possibility that a high molecular weight component is present in a large amount, the state of dispersion of the modifier is reduced. For this purpose, the coefficient of determination was improved by incorporating the molecular weight ratio, that is, the molecular weight distribution, into the formula. In particular, in the asphalt shown in Comparative Example 6, A
It shows a very small value of S / AR = 0.03, and although there are many dissolved components of the modifying material and few dissolution inhibiting components,
It is considered that the storage stability and the modification effect are inferior to those of Examples 4 to 7 due to the molecular weight and molecular weight distribution.

【0032】以上より、本発明の実施例1〜7が舗装用
改質アスファルト組成物として効果的であると言える。
本発明は、改質アスファルトのベースとなるアスファル
ト類の平均分子量がある程度小さく、また高分子量成分
が少ないほど、改質材の分散性が良好になり、改質効果
も大きくなり、さらに改質材の溶解成分としての芳香族
分と溶解阻害成分としてのアスファルテンの比により改
質効果が異なるという知見に基づいたものでる。例え
ば、SBSとアスファルトの混合が、SBSのポリマー
鎖中にアスファルト分子が入り込み、絡みつくことによ
り成されるものと考察すると、分子量が小さいアスファ
ルト類は、容易にポリマー鎖と混じり合うことができる
が、分子量が大きいアスファルト類、あるいは高分子量
成分が多いアスファルト類は、その高分子量成分が、そ
のようなポリマー鎖との混合を、立体的に阻害するため
に相溶性が低下するものと考えられる。さらに、溶解阻
害成分としてのアスファルテンが多くても、可塑剤添加
により、アスファルト類の組成を変化させて、改質材の
溶解性を向上することが可能となる。
From the above, it can be said that Examples 1 to 7 of the present invention are effective as a modified asphalt composition for pavement.
In the present invention, the average molecular weight of the asphalt as the base of the modified asphalt is small to some extent, and the less the high molecular weight component, the better the dispersibility of the modifying material, the greater the modifying effect, and the more the modifying material Is based on the finding that the modifying effect differs depending on the ratio of the aromatic component as a dissolution component to asphaltene as a dissolution inhibiting component. For example, considering that the mixture of SBS and asphalt is formed by asphalt molecules entering into the polymer chains of SBS and entangled, asphalts having a small molecular weight can easily mix with the polymer chains. It is considered that asphalts having a large molecular weight or asphalts having a high molecular weight component have a low compatibility because the high molecular weight component sterically hinders mixing with such a polymer chain. Furthermore, even if there is a large amount of asphaltene as a dissolution inhibiting component, the addition of a plasticizer can change the composition of asphalts and improve the solubility of the modifier.

【0033】[0033]

【発明の効果】本発明の舗装用改質アスファルト組成物
は、ベースとなるアスファルト類と改質材との相溶性が
良く、アスファルト舗装の耐轍掘れ性と相関が高いとさ
れる60℃粘度、及びアスファルトバインダーと骨材の
接着性とバインダー同志の結合力の指標となるタフネス
の優れた性能を示し、加熱貯蔵安定性に優れている。従
って、本発明の舗装用改質アスファルト組成物は、実用
上極めて有用である。
The modified asphalt composition for pavement of the present invention has a good compatibility between the base asphalts and the modifying material, and a viscosity at 60 ° C. which is considered to have a high correlation with the asphalt pavement resistance to rutting. And excellent toughness, which is an index of the adhesion between the asphalt binder and the aggregate and the bonding strength between the binders, and is excellent in the heat storage stability. Therefore, the modified asphalt composition for paving of the present invention is extremely useful in practice.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 高木 清美 埼玉県幸手市権現堂1134−2 株式会社コ スモ総合研究所研究開発センター内 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Kiyomi Takagi 1134-2 Gongendo, Satte City, Saitama Prefecture, Cosmo Research Institute R & D Center

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】式(1)を満たし、かつアスファルテン分
量が0〜30質量%、芳香族分量が1〜100質量%で
あるアスファルト類に改質材として、ゴム、熱可塑性エ
ラストマー、及び樹脂のうち少なくとも1種が配合され
ており、配合されているときのゴム、熱可塑性エラスト
マー、又は樹脂の含有量がそれぞれアスファルト類と前
記各改質材の合計量の2〜40質量%であることを特徴
とする舗装用改質アスファルト組成物。 【数1】 Z1>0.4 ・・・・(1) Z1=+3.07−3.28×MN/1000−2.1
9×AS/AR (式中、MNは数平均分子量、ASはアスファルテン質
量%、ARは芳香族分質量%を示す。)
1. Asphalts satisfying the formula (1) and having an asphaltene content of 0 to 30% by mass and an aromatic content of 1 to 100% by mass as rubber, thermoplastic elastomer and resin as modifiers. At least one of them is compounded, and the rubber, thermoplastic elastomer, or resin content when compounded is 2 to 40% by mass of the total amount of asphalts and each of the modifiers. Characteristic modified asphalt composition for pavement. (1) Z1 = + 3.07−3.28 × MN / 1000−2.1
9 × AS / AR (wherein, MN represents number average molecular weight, AS represents asphalten mass%, and AR represents aromatic mass%).
【請求項2】式(2)を満たし、かつアスファルテン分
量が0〜30質量%、芳香族分量が1〜100質量%で
あるアスファルト類に改質材として、ゴム、熱可塑性エ
ラストマー、及び樹脂のうち少なくとも1種が配合され
ており、配合されているときのゴム、熱可塑性エラスト
マー、又は樹脂の含有量がそれぞれアスファルト類と前
記各改質材の合計量の2〜40質量%であることを特徴
とする舗装用改質アスファルト組成物。 【数2】 Z2>0.4 ・・・・(2) Z2=+0.14−2.95×AS/AR−1.54×
MW/1000+1.37×MW/MN (式中、MNは数平均分子量、MWは重量平均分子量、
ASはアスファルテン質量%、ARは芳香族分質量%を
示す。)
2. Asphalts satisfying the formula (2) and having an asphaltene content of 0 to 30% by mass and an aromatic content of 1 to 100% by mass are used as modifiers for rubbers, thermoplastic elastomers and resins. At least one of them is compounded, and the rubber, thermoplastic elastomer, or resin content when compounded is 2 to 40% by mass of the total amount of asphalts and each of the modifiers. Characteristic modified asphalt composition for pavement. ## EQU2 ## Z2> 0.4 (2) Z2 = + 0.14-2.95 × AS / AR-1.54 ×
MW / 1000 + 1.37 × MW / MN (where, MN is a number average molecular weight, MW is a weight average molecular weight,
AS indicates asphalten mass%, and AR indicates aromatic mass%. )
JP36163197A 1997-12-11 1997-12-11 Modified asphalt composition for paving Expired - Fee Related JP4067161B2 (en)

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Application Number Priority Date Filing Date Title
JP36163197A JP4067161B2 (en) 1997-12-11 1997-12-11 Modified asphalt composition for paving

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JPH11172111A true JPH11172111A (en) 1999-06-29
JP4067161B2 JP4067161B2 (en) 2008-03-26

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ID=18474352

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