New composite grouting materials:Modified urea-formaldehyde resin with cement

A new composite two component grout comprised of modified urea-formaldehyde resin and cement was formulated to take account of the advantages and disadvantages of both the cement grout and the chemical grout.The new grout is designed for water blocking by reinforcing as well as seepage control by bore grouting.The A component consists of a modified urea-formaldehyde resin A component,some cement,and some water.The B component is an alkaline coagulant.An orthogonal test of four factors at three levels showed that gel time increased with increased water content and with urea-formaldehyde resin content.Gel time decreased at increased levels of alkaline coagulant.The A component of this new composite grout is stable over time.A mixed cross-over test showed that as the volume ratio of A to B increases the gel time falls at first but then increases.The solid strength decreases with increasing levels of the B component.The solid strength increases over time and becomes stable by the 28th day after mixing.The viscosity increases with increasing levels of resin A component.The increase is exponential and may be fit to:l = 8.162e0.0286x.

STUDIES ON IPE OF POLYACRYLAMIDE INVERSE EMULSION AND MODIFIDE UREA-FORMALDEHYDE RESIN

The selective water plugging agent was prepared by heating the blends of the polyacry-lamide inverse latex, modified urea formaldehyde resin, crosslinking agent and catalysts.The results show that using different types of polymers and additives or changing in theirproportion of the blends, the gelling viscosity, starting point of gelling and other propertiesof the IPN can be controlled.

Curing Reaction Kinetics of Epoxy Resin Using Dicyandiamide Modified by Aromatic Amines

The curing reaction and reaction mechanism of epoxy resin E-44, for which aromatic amine modified dicyandiamide was used as a curing reagent, were investigated by means of differential scanning calorimetry （DSC）. The results showed that the modified dicyandiamide had better curing characteristic than unmodified dicyandiamide for epoxy resin E-44, and the curing reaction could be carried out at moderate temperature. Apparent activation energy of the curing reaction was decreased appreciably from 123.829 kJ/mol to 61.550-64.405 kJ/mol, and reaction order was decreased from 0.941 to 0.896-0.900. Curing reaction mechanism also was discussed.

DynamicMechanical and Chemorheology Analysis for the Blended Epoxy System with Polyurethane Modified Resin

As the important matrix material,epoxy resin has been widely used in the composites for various fields.On account of the poor toughness of epoxy resin limiting their suitability for advanced applications,considerable interests have been conducted to modify the epoxy resin to meet the engineering requirements.In this study,the bio-based polyurethane(PU)modified resin was adopted to modify the pure bisphenol-A epoxy by blending method with various proportions.Aiming to illuminate the curing behavior,mechanical and thermal properties,the blended epoxy systems were characterized by viscosity-time analysis,dynamic mechanical analysis(DMA)at different frequencies and temperatures,mechanical tensile test,thermogravimetric analysis(TGA)and Fourier transform infrared(FT-IR)spectroscopy.The results indicated that the introduction of PU modified epoxy was found to significantly inhibit the viscosity growth rates especially when the content of PU modified epoxy resin is higher than 60%.Notwithstanding the dynamic modulus and T_(g)reduced with the increment of PU modified epoxy,remarkable increment on the elongation at break was found and the flexibility was greatly promoted with the introduction of PU modified epoxy.The proportion of PU modified epoxy in the blends should be put balance considerations to obtain optimal mechanical properties.TGA results and FTIR spectrum demonstrated that the addition of PU modified epoxy did not change the thermal decomposition mechanism and chemical reaction mechanism,but the addition of PU modified epoxy inhibits the curing reaction of epoxy resin by measured and calculated the damping temperature domain
T from 35.7℃ to 48.9℃.

Synthesis of modified D401 chelating resin and its adsorption properties for Pb^(2+)

A novel chelating resin with sulfonic group was synthesized by chemical modification of D401 resin with sulphonation reaction and characterized by FT-IR spectrometry. The adsorption properties of the novel chelating resin for Pb2+ were studied by batch adsorption, and the adsorption process was analyzed from thermodynamics and kinetics aspects. The adsorption mechanism of Pb2+ on the modified D401 chelating resin was discussed by FT-IR spectrometry. Experimental results show that in the Pb2+ concentration range of 200-400 mg/L, the adsorption capacities of the modified D401 chelating resin for Pb2+ increase by 77%-129%, and Langmuir isothermal adsorption model is more suitable for the equilibrium adsorption data. Adsorption is an endothermic process that runs spontaneously. Kinetic analysis shows that the adsorption rate is mainly governed by liquid film diffusion. The best pH value under adsorption condition is 4-5. The saturated resin can be regenerated by 3 mol/L nitric acid, and the adsorption capacity remains stable after five consecutive adsorption-desorption cycles. The maximal static saturated adsorption capacity of the resin is 206 mg/g at 333 K in the Pb2+ concentration range of 200-400 mg/L. The modified D401 chelating resin is an efficient adsorbent for the removal of Pb2+ from its single-metal ion solution.

Preparation, morphology and mechanical properties of acrylate-modified polyurethane/unsaturated polyester resin graft-IPNs

Acrylate modified polyurethane resin was first synthesized, and interpenetrated with unsaturated polyester resin to form IPNs and gradient IPNs which cured at room temperature. The polymerization process was traced by an IR spectroscopy technique and the simultaneous interpenetrating techniques were determined. The morphology of these IPNs were estimated by TMA and TEM methods. The results indicated that large amount of interpenetrating and entanglement make T g  linked up effectively, and domains between two phases can be in nanometre ranges, which changed with composition ratios. The mechanical properties results showed that IPNs varied from elastomeric to plastic materials. It was noteworthy that, with the introduction of modified groups and the formation of graft construction in IPNs, the miscibility in the systems was improved a lot. These further led to the improved mechanical properties of IPNs with elastomer reinforced and plasticizer toughened as well. The reinforced miscibility between the networks can apparently change mechanical property especially for the gradient ones when the materials are elongated.

Study on direct-chain diacid modified phenolic resin for Al-alloy casting

Resin coated sand (RCS) with phenolic resin matrix can hardly be collapsed when it is used in Al-alloy casting. Adding collapsing agent and reducing the concentration of resin are solutions adopted by workers, but these methods tend to reduce the initial strength of RCS. Synthesis of modified phenolic resin with direct-chain diacid DAn (/JS=6, where n means carbon amount) was studied here. The effects of the addition of modifying agent on molecular weight, gel time and softening point were investigated. Optimal addition of DAn (10% phenol) was obtained by testing the initial and retained flexural strengths of the modified resin. FT-IR spectra showed that carbonyl shifts to higher wave number. With the use of TG, SEM and strength loss curves, the relation between initial and retained strengths was analysed. Tests on the heated deformation curve, before and after resin modification, show that PF-DA10 has the characteristic of higher initial and retained strengths together.

Study on Preparation of Waterproofing Agent for Mineral Wool Board from Modified C_9 Petroleum Resin

The modified petroleum resin emulsion prepared from the C9petroleum resin was modified with maleic anhydride.The effects of maleic rosin and maleic anhydride addition level,the modification time and the alkali liquor on the properties of the emulsion were discussed.The results showed that the optimum process conditions covered:a maleic anhydride mass fraction of 1.5%,a maleic rosin mass fraction of 10%,a KOH mass fraction of 1%,a petroleum resin modification temperature of 200℃,a petroleum resin modification duration of 3 h,and a modified petroleum resin emulsion/wax emulsion mixing ratio of 1:1.The particle size of modified petroleum resin emulsion prepared under these conditions was equal to 104.166μm.

Research of Lignin Modified Phenol Formaldehyde Resin Bonded Magnesia Carbon Bricks

In order to reduce the cost and to improve the low temperature bonding strength of phenol formaldehyde resin（ PF）,the lignin modified phenol formaldehyde resin（ LPF） was synthesized using calcium lignosulfonate as a partial replacement of phenol,and sodium hydroxide as catalyzer. Then the magnesia carbon bricks were prepared using the LPF as binder. Different process conditions of LPFs such as calcium lignosulfonate additions（ 10%,20%,30%,40% and 50%,in mass,the same hereinafter）,catalyzer additions（ extra added,1%,2%,3%,4% and 5%） and reaction times（ 1,1. 5,2,2. 5 and 3 h） were investigated. Effects of prepared LPFs on properties of magnesia carbon bricks（ baked at 200 ℃ for 24 h） were researched in order to modify the synthesizing conditions of LPFs. Cold physical properties and hot modulus of rupture of magnesia carbon bricks bonded by LPF and by traditional PF after baked at 200 ℃ for 24 h and fired at 1 200 ℃ for 3 h were compared,respectively. The results show that the optimal synthesizing conditions of LPF for preparing magnesia carbon bricks are 30% calcium lignosulfonate,1% catalyzer,and 2 h reaction time. The magnesia carbon bricks bonded by the optimal LPF achieve：（ 1） the bulk densities 2. 84 g · cm- 3and 2. 82g·cm- 3,apparent porosities 9. 6% and 14. 6%,moduli of rupture 17. 8 MPa and 6. 4 MPa,crushing strengths72. 3 MPa and 48. 7 MPa,after baked at 200 ℃ and1 200 ℃,respectively;（ 2） the hot modulus of rupture7. 3 MPa after fired at 1 400 ℃. The above properties are better than those of the magnesia carbon brick bonded by PF.

Short Communication—A Novel Sample Preparation Method That Enables Ultrathin Sectioning of Urea-Formaldehyde Resin for Imaging by Transmission Electron Microscopy

Urea-formaldehyde (UF) resin is widely used as an adhesive for the manufacture of a range of wood and fiber based products. Although the microstructure of this resin has been examined at high resolution by field-emission scanning electron microscopy and atomic force microscopy, transmission electron microscopy (TEM) has thus far not been used, perhaps because of difficulties in ultrathin sectioning this resin in cured (polymerized) state. In the technical note presented here, a novel sample preparation method is described which enabled us to examine the microstructural morphology of UF resin by transmission electron microscopy in ultrathin sections, revealing the presence of spherical particles within the resin. Our initial attempt to ultrathin section the resin directly was not successful as it was too brittle to trim blocks for sectioning. Then, we developed a sample preparation technique that involved impregnation ofPinus radiatawood tissues with the UF resin, and then embedding of resin impregnated wood tissues with Spurr’s low viscosity embedding medium, which has been widely employed in plant and wood ultrastructure work. The TEM images illustrated and the information on the microstructural morphology of the UF resin presented are based on this novel sample preparation approach.

STUDIES ON THE ADSORPTION OF PHENOLIC COMPOUNDS ON A PS-BASED RESIN MODIFIED BY NITRO FUNCTIONAL GROUPS

A new adsorbent (JN-01) was prepared by modifying resin NDA-1800 with nitro functional groups.The adsorption capacities of resins XAD-4,NDA-1800 and JN-01 were investigated,and the results indicated that the modified resin JN-01 was much better in adsorbing phenol,p-nitrophenol and p-cresol.The adsorption capacities of the resin JN-01 were higher than those of the resins XAD-4 and NDA-1800 within a temperature range of 283-323 K,which might be attributed to the higher surface area and the partial polarity o...

The Evaluation of a Resin-modified Glass Ionome Cement for Bonding Orthodontic Brackets

To evaluate the shear bond strength（SBS） and bond failure interface after the debonding of orthodontic brackets with a resin-modified glass ionomer cement（RMGIC） under six bonding conditions, 140 premolar teeth were randomly divided into seven groups. The brackets of all groups, except for control group, were bonded using a RMGIC. The teeth were debonded using a universal testing machine. The shear bond strength, adhesive remnant index （ARI） and enamel fracture were examined for each debonding. A significant difference existed in SBS under wet and dry conditions in two groups of Fuji Ortho LC. Different degree of enamel fracture was seen in groups of Fuji Ortho LC（dry/37% phosphoric acid treated） after debonding. Bond failed predominantly at the enamel-adhesive interface, except for phosphoric acid treated groups. The RMGIC achieve a clinically effective adhesion in orthodontics under different bonding conditions.

Compatibility evaluation between waterborne epoxy resin and SBR latex modified asphalt emulsion

Good compatibility between waterborne epoxy resin(WER)modifier and styrene-butadiene rubber(SBR)latex modified asphalt emulsion(SBRE)is an essential premise for good pavement performance of WER and SBR latex compositely modified asphalt emulsion(WSAE).This study aims to explore the compatibility between WER modifier and SBRE.To achieve the goal,several WER modifiers produced by two methods were first selected to modify SBRE,thus the WSAEs were prepared.Next,storage stability and workability of the WSAEs themselves,and high-temperature performance,rheological behavior and temperature sensitivity of their evaporated residues were compared and evaluated via performing a series of experiments,respectively,thus the WER modifier possessing an optimal modification effect was recommended.Results show that the storage stability of WSAEs is sensitive to the amount of WERs.The incorporation of 1%WERs by the mass of SBRE improves the storage stability of SBRE,while WERs that exceed 1%weaken its storage stability.When the WERs reach 3%and 4%,the 5 d storage stability of prepared WSAEs will be beyond the limitation of specification.Incorporating WERs into SBRE negatively affects the workability of SBRE,and the workability of WSAEs is adversely influenced by the WERs content and the storage time.To ensure the construction,the WSAEs with 3%and 4%WERs should not be stored for more than 36 h and 48 h,respectively.The WERs effectively improve the high-temperature performance of SBRE residue,especially the 3%WERs.Besides,the WERs notably enhance the rheological property and thermal stability of SBRE residue.In contrast,the WER modifier produced by chemically modified method has a smaller adverse impact on the storage stability and workability of WSAE,and a larger enhancement on the high-temperature performance,rheological property and thermal stability of SBRE residue,which is thus recommended to modify SBRE.

TRIMETHYLSILYLATED SILICA AS RHEOLOGY MODIFIER FOR SILICONE RESINS

Trimethylsilylated silica was synthesized. through hydrolytic condensation of tetraethoxysilane followed by trimethylsilylation. Rheological properties of the silicone resin with trimethylsilylated silica as modifier were studied. It turned out that the particle size of silica was important to the rheological behavior of the modified resin. Trimethylsilylated silica of medium particle size shows the strongest tendency of forming physical network in the resin.

玉米秸秆焦油制备生物沥青的性能研究

随着大规模高等级公路建设和养护维修工程的不断推进,沥青材料的需求量逐渐攀升。随着化石资源的消耗,寻找一种能够替代石油沥青的材料已成为道路工程领域的迫切需求。本文以玉米秸秆焦油为原料,对其进行树脂化处理,制备生物沥青。基于BOX-Behnken响应面分析,以树脂得率为评价指标,确定了树脂合成的最佳工艺条件为:酚醛摩尔比为0.8,反应时间为125 min,秸秆焦油添加量为10%。结果表明:随着树脂化产物的增加,生物沥青的针入度也随之增大,且均高于70#石油沥青。B-PF生物沥青延度随掺量增加呈先升高后降低趋势;但H-PF生物沥青延度随掺量的增大而减小。提高生物沥青掺量可使软化点降低。H-PF生物沥青在10%掺量下延度及软化点低于70#石油沥青,而掺量达到20%时,所制备的生物沥青的软化点和延度皆低于70#石油沥青。

含聚硅氧烷链段邻苯二甲腈树脂的制备及性能

以端羟基聚二甲基硅氧烷和4-硝基邻苯二甲腈为原料,在强极性溶剂中进行亲核取代反应合成了含聚硅氧烷链段邻苯二甲腈树脂(SIPH),并利用氨基改性剂(AWL)与该树脂进行反应制备了改性含聚硅氧烷链段邻苯二甲腈树脂预聚物(SIPH-AL)。通过红外光谱和核磁共振表征了SIPH树脂的化学结构;采用差示扫描量热法、红外光谱法、热重分析和动态力学热分析表征了SIPH-AL的固化行为和固化物的耐热性。结果表明,SIPH-AL起始固化温度为207℃,其固化物在空气和氮气中失重5%的温度(T_(d5))及1000℃质量保留率分别是453℃,29%和500℃,77%;石英纤维增强SIPH-AL复合材料室温和600℃时的弯曲强度分别为515.5 MPa和94.5 MPa,玻璃化转变温度(T_(g))高于500℃。

水性有机硅改性环氧树脂的制备与性能

利用二甲基二氯硅烷(DMDCS)与环氧树脂E51中-OH缩合反应合成有机硅改性环氧树脂,并采用相反转法制备水性有机硅改性环氧树脂,以疏水性优选有机硅改性环氧树脂合成条件,分析了乳化工艺对乳液平均粒径的影响,并考察了固化膜性能。结果表明,在环氧树脂40 g、DMDCS 1.6 g、溶剂用量20 mL、50℃反应8 h的条件下,有机硅改性环氧树脂与水的接触角为106.8°;当乳化剂用量为25%、乳化温度为65℃、剪切机转速为3000 r/min时,乳液平均粒径为1.011μm,储存稳定性(30 d)和离心稳定性(3000 r/min,30 min)良好;水性有机硅改性环氧固化膜固化时间短,具有优良的疏水性、力学性能、耐腐蚀性能。

促牙本质再矿化树脂粘接材料提高牙本质粘接耐久性的研究进展

促进牙本质再矿化是提高树脂-牙本质粘接耐久性的重要方法,国内国际有很多关于改性树脂粘接剂的研究,均致力于诱导混合层裸露牙本质胶原的再矿化。本文针对树脂-牙本质粘接面的耐久性问题,阐述了促牙本质再矿化树脂粘接材料的研究进展。促牙本质再矿化树脂粘接材料的改性策略包括:生物活性无机微填料策略,即以硅酸盐、磷酸钙盐和生物活性玻璃等无机材料为矿化离子来源诱导牙本质再矿化;仿生再矿化策略,即应用仿生类似物模拟非胶原蛋白(non-collagenous proteins,NCPs)的功能,引导矿物前驱体在特定位点矿化以获得与生物矿化类似的有序晶体沉积;以及锌添加剂保护胶原蛋白、介孔硅材料作为矿物离子输送系统的改性策略。

氨基水杨酸改性单宁基树脂的制备及其对Ag(I)的吸附

以杨梅单宁为原料,采用氯代的方法制备得到氯化单宁,再与氨基水杨酸反应得到氨基水杨酸改性单宁,然后经多聚甲醛交联得到氨基水杨酸改性单宁基树脂.采用傅里叶变换红外光谱仪对氨基水杨酸改性单宁基树脂的结构进行表征,并探究了溶液pH值、Ag(I)初始质量浓度、温度、时间等因素对氨基水杨酸改性单宁基树脂吸附性能的影响.结果表明,在温度为318 K、pH值为5.0、吸附时间为7 h、Ag(I)初始质量浓度为260 mg/L时,氨基水杨酸改性单宁基树脂对Ag(I)的最大吸附量可达239.6 mg/g,吸附过程符合Langmuir吸附等温模型和准二级动力学模型.这说明氨基水杨酸改性单宁基树脂具有良好Ag(I)吸附性能.