Summary of Current Quality Control/ Quality Assurance Practices for Hot-Mix Asphalt Construction

Author(s):  
Robert L. Schmitt ◽  
Jeffrey S. Russell ◽  
Awad S. Hanna ◽  
Hussain U. Bahia ◽  
Galadriel A. Jung

State highway agencies and contractors have been implementing quality control/quality assurance (QC/QA) specifications in recent years to advance the quality of hot-mix asphalt (HMA) construction. During their continued development, attributes of these QC/QA specifications have varied among states. The objective of this paper is to provide a compilation of state-of-the-practice in QC/QA for HMA construction and provide recommendations for state highway agencies and contractors when modifying or developing a QC/QA specification. Survey data from 42 state highway agencies and 61 contractors working within 14 states found that a majority of states are using contractor data for acceptance. A review of QC/QA specifications from 40 states found that most states are using plant-produced mix properties, density, and smoothness tests to determine overall quality and acceptance of HMA construction work. A larger number of states are using quality level analysis for specification compliance by estimating percent within limits or percent defective for mix properties and density. Consideration is given to key attributes of a QC/QA specification, including ( a) whether to use contractor or agency data for acceptance, ( b) use of quantity or time for lots, and ( c) testing frequency. State highway agencies and contractors may find this report useful for understanding the components of different QC/QA specifications and furnishing essential information as both parties collaborate during specification development.

Author(s):  
Robert P. Elliott ◽  
Yanjun Qiu

A common provision in quality control/quality assurance construction contracts is the adjustment of the contractor's pay on the basis of the quality of the construction. The expected impact of the provision on the pay should be examined to ensure that the adjustments are neither unduly severe nor excessively lenient. Most pay adjustment plans have been developed around a quality index by using a percent defective approach. Analyses of these plans are complex but reasonably well defined. Other plans, however, are more complex and do not lend themselves to direct analysis. These plans can be examined by computer simulation. The use of computer simulation to examine a complex pay adjustment provision is demonstrated. The analyses show that simulation can reveal that a pay adjustment schedule behaves differently than it appears on the surface. For example, the schedule examined bases pay solely on averages and appears to ignore construction variability. The analyses, however, demonstrate that the pay adjustments are at least as sensitive to construction variability as they are to construction averages. It is also shown that the simulation process can provide a better, more detailed examination of the pay schedule than is possible by simply determining the expected pay. In particular, the simulation process can provide an indication of the variability of pay at various quality levels and can identify the factors most responsible for pay adjustments.


KREATOR ◽  
2021 ◽  
Vol 2 (1) ◽  
Author(s):  
Soebardianto . ◽  
Septia Ardiani ◽  
Romi Setiawan

The quality control activities, in particular the measurement of density values, are part of the quality control parameters carried out by each company. Companies sometimes forget about the quality parameters of the name, even though the quality can give the printed products a good guarantee in the eyes of consumers. To achieve the quality level, of course, the business does not stand idle, there are several things that need to be done or provided by the business to support the quality, namely man (human), machine (machine), material (material), and method (method). In the development of technology in an increasingly advanced digital world, companies want to continue to compete with a digital world by making inroads, this of course gives the products produced by the company a good or a good level of quality. In this discussion, there is an identification of problematic aspects arising from the deviation of density values as well as ways to obtain standard density values and factors that affect the quality of prints on book cover prints using a Heidelberg machine.Keywords—Quality Control, Density, Standart, Product, Deviation


2019 ◽  
Vol 14 (3) ◽  
pp. 605-613 ◽  
Author(s):  
Parastou Kharazmi

Abstract Water and wastewater pipes require some of the highest levels of infrastructure investment; they also deteriorate faster than they can be repaired. The use of alternative rehabilitation technologies, which are quicker and less expensive than pipe replacement, has therefore increased significantly in recent years, worldwide. Field studies on relined wastewater pipes removed from buildings in different parts of Sweden revealed the existence of a variety of common defects, most of which could have been prevented by better installation. Increased quality-focused monitoring could help to ensure that relined pipes reach their expected service life, while comprehensive documentation could assist in providing sufficient information to facilitate progress in the field. This paper includes a brief overview of the technologies used in Sweden, current quality control practices, repeated observed defects related to installation, crucial steps that affect final quality, and recommendations to be considered in the contexts of detailed quality control and quality assurance procedures.


2019 ◽  
pp. 66-72
Author(s):  
O. A. Zdoryk

Formulations and in-pharmacy preparation process of compounded drugs were being created for centuries, and seem to have no concerns regarding the quality, compatibility and stability during storage or usage. Taking in mind modern trends for quality assurance and standardization of drugs, quality of preparation process of compounded drugs can be proved by using of a systematic approach that is based on pharmaceutical quality systems. Variability of preparation conditions, preparation equipment from pharmacy to pharmacy, personal professional skills require the development of defined standards, rules and summarized the strategy of quality assurance of compounded drugs. The aim of this paper was determination of critical factors and development of the design for quality assurance of compounded drugs. The materials of this study were the regulative base of Ukraine, international documents, guidances and own investigations concerning the requirements for the preparation process and quality control of compounded drugs. The methods used were data systematical analysis, bibliosemantic and summary. The achievement of good quality of compounded drugs can be present as a step-by-step process, that cover adherence to necessary preparation procedure and knowledge of peculiarities of drugs, process understanding, identification of risks and its evaluation, minimization and implementation of the quality management system for documentation, equipment and personnel. As a result of preparation schemes analysis, the critical factors were determined and the Fishbone diagram was proposed. The factors contributing to the general strategy of compounded drugs quality assurance, such as prescription analysis, personnel, regulative base, conditions of preparation process and equipment, documentation, dispensing, characteristics of active ingredients and additives, compounding design, preparation technology, containers and package, quality control, stability and labelling were determined. The proposed diagram of causes and effects can be used as a template for the identification and quantification of risks during preparation and quality control of compounded drugs. The proposed general scheme for quality assurance is necessary for organization and optimization of monitoring preparation and quality control, implementation of remedial and preventive measures, tracking of causes, nonconformities, and prevention of its repetition, management of variables, determination of improvement possibilities and audit conducting.


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